CN108997351A - Containing substitution to chloro acetyl piperazine compounds and the preparation method and application thereof - Google Patents
Containing substitution to chloro acetyl piperazine compounds and the preparation method and application thereof Download PDFInfo
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- CN108997351A CN108997351A CN201810790461.1A CN201810790461A CN108997351A CN 108997351 A CN108997351 A CN 108997351A CN 201810790461 A CN201810790461 A CN 201810790461A CN 108997351 A CN108997351 A CN 108997351A
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- 0 CCC*(CC*C1=*C=**2*3(CC3)C(C)*C12)C(*c1ccc(*)cc1)=* Chemical compound CCC*(CC*C1=*C=**2*3(CC3)C(C)*C12)C(*c1ccc(*)cc1)=* 0.000 description 4
- LWQLLIVTGSMSCT-UHFFFAOYSA-N COC(C(c(cc1)ccc1Cl)Br)=O Chemical compound COC(C(c(cc1)ccc1Cl)Br)=O LWQLLIVTGSMSCT-UHFFFAOYSA-N 0.000 description 1
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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Abstract
The application provides one kind containing replacing to chloro acetyl piperazine compounds and the preparation method and application thereof, such compound has structure shown in formula (I):
Description
Technical field
This application involves organic compound synthesis and medical applications fields, and in particular to one kind is containing substitution to chloro acetyl
Piperazine compounds and its preparation method and application.
Background technique
The separation for deeply starting from two genes Akts 1 and Akt2 of Akt research, they are the people of viral oncogenes v-akt
Class homologous gene, the protein and PKC and PKA very high homology of coding, therefore also referred to as PKB.(referring to: Manning, B.D.;
Toker, A.AKT/PKB Signaling:Navigating the Network.Cell2017,169,381-405.) Akt is
A kind of serine/threonine protein kitase, the crystal structure in conjunction with ATP were illustrated early in 2005.Akt belongs to AGC
Family member contains 480 amino acid, and there are three kinds of hypotypes, i.e. Akt1 (PKB α), Akt2 (PKB β) and Akt3 (PKB γ).
(referring to: Osaki, M.;Oshimura,M.;Ito,H.PI3K-Akt pathway:its functions and
Alterations in human cancer.Apoptosis2004,9,667-676.) three have similar structure: a N
Domain pleckstrin homology (pleckstrin homology, PH) of end, a centrally located kinase catalytic domain
The prolongation (EXT) of (CAT domain) and an end C-, EXT contain the hydrophobic motif of a regulation
(hydrophobic motif,HM).These three hypotypes, it is homologous in the domain PH about 80%, connect the linker in the domain PH and catalytic domain
17 about 46% is homologous, and catalytic domain about 90% is homologous, and C- terminal extension part (EXT) about 70% is homologous.(referring to: Kumar, C.C.;
Madison,V.AKT crystal structure and AKT-specific inhibitors.Oncogene 2005,24,
7493-7501.)
PI3K/AKT/mTOR signal path plays quite crucial effect in cell survival and growth, is tumour cell
Resist one of the important access of cell death.(referring to: De, L.A.;Maiello,M.R.;D'Alessio,A.;Pergameno,
M.;Normanno,N.The RAS/RAF/MEK/ERK and the PI3K/AKT signalling pathways:role
in cancer pathogenesis and implications for therapeutic approaches.Expert
Opin Ther Targets2012,16Suppl 2:S17.) Akt is pass in cell Proliferation, survival, apoptosis and metabolic regulation
Key node, after Akt is activated, more than 100 kinds of phosphorylatable downstream substrate plays its biological function, inhibits the Akt to be beneficial to
The targeted therapy of tumour.(referring to: Manning, B.D.;Cantley,L.C.AKT/PKB signaling:navigating
Downstream.Cell2007,129,1261.) have become the heat of research using Akt as the research of the anti-tumor drug of target spot at present
One of point.
Summary of the invention
Contain this application provides one kind and replaces to chloro acetyl piperazine compounds and its preparation method and application, such
Compound has inhibitory activity to the growth of Akt1 kinases and MCL cell strain.
The application is achieved by the following technical solution:
Firstly, this application provides compound shown in a kind of formula (I) or its isomers or solvate or officinal salt:
Wherein, X is selected from H ,-CH- ,-C-Br and halogen;Y is selected from H ,-CH-, C1-C18Linear or branched alkyl group;X and Y it
BetweenFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, contain one or more
A heteroatomic five yuan or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;
Further, X is selected from H ,-CH- ,-C-Br and halogen;Y is selected from H ,-CH- and C1-C8Linear or branched alkyl group;X
Between YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, contain one or more
A heteroatomic five yuan or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;
Further, X is selected from H ,-CH- ,-C-Br, F, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear chain or branched chain alkane
Base;Between X and YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from amino, substituted-amino, cyano, containing one or more heteroatomic
Five yuan or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;Wherein, the substituted-amino be by tertbutyloxycarbonyl (Boc) and/
Or C1-C18Linear or branched alkyl group replaced amino;Wherein, described containing one or more heteroatomic five yuan or hexatomic rings
Alkyl is selected from pyrroles, piperidines, substituted piperidine, morpholine, piperazine and substituted-piperazinyl;
Further, X is selected from H ,-CH- ,-C-Br, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X
Between YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from amino, substituted-amino, cyano, containing one or more heteroatomic
Five yuan or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-
C8Linear or branched alkyl group replaced amino;It is described to be selected from pyrrole containing one or more heteroatomic five yuan or hexa-atomic naphthenic base
It coughs up, piperidines, substituted piperidine, morpholine, piperazine and substituted-piperazinyl;
Further, the substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Linear chain or branched chain alkane
Base, amino, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, X is selected from H ,-CH- ,-C-Br, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X
Between YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from amino, substituted-amino, containing one or more heteroatomic five yuan
Or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C3's
Amino replaced linear or branched alkyl group;It is described containing one or more heteroatomic five yuan or hexa-atomic naphthenic base be selected from pyrroles,
Piperidines, substituted piperidine, morpholine, piperazine and substituted-piperazinyl;The substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5
Linear chain or branched chain alkyl, amino, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, the substituted-amino is selected from
Further, the substituted piperidine is selected from
Further, the substituted-piperazinyl is selected from
Further, X is selected from H ,-CH- ,-C-Br, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X
Between YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2It is selected from
Further, in formula (I), when being double bond between X and Y, X is-C-Br, when Y is-CH-, R1It is not
Further, in one or more embodiments, between X and YFor double bond, X is selected from-CH- and-C-Br;
Y is-CH-;
Further, the compound has structure as follows:
Wherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or six
First naphthenic base, the hetero atom are selected from O, S and N;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C18Linear chain or branched chain
Amino replaced alkyl;It is described to be selected from pyrroles containing one or more heteroatomic five yuan or hexa-atomic naphthenic base, piperidines, replace piperazine
Pyridine, morpholine, piperazine and substituted-piperazinyl;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C8Linear chain or branched chain
Amino replaced alkyl;It is described to be selected from pyrroles containing one or more heteroatomic five yuan or hexa-atomic naphthenic base, piperidines, replace piperazine
Pyridine, morpholine, piperazine and substituted-piperazinyl;
Further, the substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Linear chain or branched chain alkane
Base, amino, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, the substituted-amino is selected from
Further, the substituted piperidine is selected from
Further, the substituted-piperazinyl is selected from
Further, R2It is selected from
Further, R2It is selected from
Further, R2For
Further, in one or more embodiments, between X and YFor no key;X is selected from H and halogen;Y is
C1-C18Linear or branched alkyl group;
Further, R1For
Further, the compound has structure as follows:
Wherein, X is selected from H, F, Cl, Br;Y is C1-C8Linear or branched alkyl group;
Further, X is selected from H, F, Cl, Br;Y is C1-C5Linear or branched alkyl group;
Further, X H, Cl or Br;Y is methyl, ethyl, isopropyl or tert-butyl;
Further, X is Cl or Br;Y is methyl, ethyl, isopropyl or tert-butyl
Further, X H;Y is methyl, ethyl, isopropyl or tert-butyl;
Further, X Cl;Y is methyl, ethyl, isopropyl or tert-butyl;
Further, X Br;Y is methyl, ethyl, isopropyl or tert-butyl.
Further, the compound or its isomers or solvate or officinal salt are selected from following compound:
Tert-butyl { 2- [4- (the bromo- 7H- pyrroles of 5- [2,3-d] pyrimidine-4-yl) piperazine -1- base] -1- (4- chlorphenyl) -2-
Oxygen ethyl } carbamate (II-1);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (diformazan ammonia
Base) ethyl ketone (II-2);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (diethylamino
Base) ethyl ketone (II-3);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (pyrroles -1-
Base) ethyl ketone (II-4);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (3,5- diformazan
Phenylpiperidines -1- base) ethyl ketone (II-5);
1- [4- (5- bromo- 7H- [2,3-d] pyrimidine-4-yl) piperazinyl] -2- (4- chlorphenyl) -2- morpholine ethyl ketone (II-6);
Tert-butyl 4- { 2- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -1- (4- chlorphenyl } -2-
Oxygen ethyl) piperazine -1- carboxylate (II-7);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (4- methyl piperazine
Piperazine base) ethyl ketone (II-8);
Tert-butyl { { 1- { 2- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -1- (4- chlorphenyl) -
2- oxygen ethyl } piperidin-4-yl } methyl } carbamate (II-9);
2- amino -1- (4- (the bromo- 7H- pyrroles of 5- [2,3-d] pyrimidine-4-yl) piperazine -1- base) -2- (4- chlorobenzene) ethyl ketone salt
Hydrochlorate (II-10);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (piperazinyl)
Acetophenone hydrochloride (II-11);
2- [4- (amino methyl) piperidin-1-yl) -1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazine
Base] -2- (4- chlorphenyl) acetophenone hydrochloride (II-12);
[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (methylamino) pyrimidine-4-yl] piperazinyl } methanone hvdrochloric acid salt
(III-1);
[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (ethylamino) pyrimidine-4-yl] piperazinyl } methanone hvdrochloric acid salt (III-2);
[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (isopropylamine) pyrimidine-4-yl] piperazinyl } methanone hvdrochloric acid salt
(III-3);
4- [6- (tert-butylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-4);
{ 4- [5- chloro- 6- (methylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone hydrochloric acid
Salt (III-5);
{ 4- [5- chloro- 6- (ethylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-6);
{ 4- [5- chloro- 6- (isopropylamine) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone hydrochloric acid
Salt (III-7);
{ 4- [6- (tert-butylamino) -5- chlorine pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone salt
Hydrochlorate (III-8);
{ 4- [5- bromo- 6- (methylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone hydrochloric acid
Salt (III-9);
{ 4- [5- bromo- 6- (ethylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-10);
{ 4- [5- bromo- 6- (isopropylamine) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone hydrochloric acid
Salt (III-11);
{ 4- [5- bromo- 6- (tert-butylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone salt
Hydrochlorate (III-12).
On the other hand, present invention also provides a kind of method for preparing compound or pharmaceutically acceptable salt thereof shown in formula (II), institutes
Stating method, reaction route (reaction route 1) carries out as described below:
Wherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or six
First naphthenic base, the hetero atom are selected from O, S and N;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C18Linear chain or branched chain
Amino replaced alkyl;It is described to be selected from pyrroles containing one or more heteroatomic five yuan or hexa-atomic naphthenic base, piperidines, replace piperazine
Pyridine, morpholine, piperazine and substituted-piperazinyl;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C8Linear chain or branched chain
Amino replaced alkyl;It is described to be selected from pyrroles containing one or more heteroatomic five yuan or hexa-atomic naphthenic base, piperidines, replace piperazine
Pyridine, morpholine, piperazine and substituted-piperazinyl;
Further, the substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Linear chain or branched chain alkane
Base, amino, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, the substituted-amino is selected from
Further, the substituted piperidine is selected from
Further, the substituted-piperazinyl is selected from
Further, R2It is selected from
Further, in one or more embodiments, which comprises
(1) it is reacted in DMF (N,N-dimethylformamide) with NBS (N-bromosuccinimide) with starting material 1
Intermediate 2;
(2) intermediate 2,1-Boc- piperazine and DIEA (N, N- diisopropylethylamine) react in DMF generates intermediate 3;
(3) intermediate 3 reacts in methanol solution with hydrogen chloride dioxane solution, takes off Boc protecting group, obtains intermediate
4;
(4) intermediate 4 is in EDCI (1- (3- dimethylamino-propyl) -3- ethyl-carbodiimide hydrochloride), HOBt (1- hydroxyl
Benzotriazole), under DIEA and DMF existence condition, after reacting with intermediate acid M, obtain formula (II) compound;And/or further
Ground is reacted with the methanol solution of obtained formula (II) compound with the dioxane solution of hydrogen chloride, obtains formula (II) chemical combination newly
Object (compound is different from participating in formula (II) compound of reaction in the step)
Further, in one or more embodiments, which comprises
(1) it is reacted in DMF (N,N-dimethylformamide) with NBS (N-bromosuccinimide) with starting material 1
Intermediate 2;
(2) intermediate 2,1-Boc- piperazine and DIEA (N, N- diisopropylethylamine) react in DMF generates intermediate 3;
(3) intermediate 3 reacts in methanol solution with hydrogen chloride dioxane solution, takes off Boc protecting group, obtains intermediate
4;
(4) intermediate 4 is in EDCI (1- (3- dimethylamino-propyl) -3- ethyl-carbodiimide hydrochloride), HOBt (1- hydroxyl
Benzotriazole), under DIEA and DMF existence condition, after reacting with intermediate acid M, obtain Formula II -1~II-9 compound;
Further, by the methanol solution of obtained compound II-1, II-7, II-9 respectively with the dioxane of hydrogen chloride
Solution reaction obtains Formula II -10~II-12 compound.
Further, in one or more embodiments, the reagent and condition of each step in above-mentioned reaction route 1 are as follows:
(a) NBS, DMF, r.t. (room temperature);(b) 1-Boc- piperazine, DIEA, DMF, 110 DEG C;(c) hydrogen chloride-dioxy six
Ring, methanol, r.t.;(d) intermediate acid M, EDCI, HOBt, DIEA, DMF, r.t.;(l) hydrogen chloride-dioxane, methanol,
r.t.。
Further, in one or more embodiments, the intermediate acid M has structure as follows:
Wherein, R2It is selected from
Further, in one embodiment, the intermediate M is obtained as follows:
Further, in one or more embodiments, the intermediate acid M is prepared into according to following reaction route
It arrives:
Wherein, R2It is selected from
Further, in one or more more specifically embodiments, the preparation formula (II) compound or its can
The method of pharmaceutical salts includes:
(1) raw material 1 is dissolved in DMF, NBS is added, 12h is stirred at room temperature, reaction is finished, reaction solution poured into ice water, mistake
Filter, filter cake are washed with water, dry, obtain intermediate 2;
(2) intermediate 2,1- tert-butoxycarbonyl-piperazine and DIEA are dissolved in dioxane, 80 DEG C of microwave reaction 2h, are depressurized
Solvent is evaporated off, water, ethyl acetate extraction is added, combined ethyl acetate is successively washed three times with water and saturated sodium chloride solution, nothing
Aqueous sodium persulfate dries, filters, and silica gel column chromatography obtains crude product, with ethyl alcohol recrystallization, obtains white solid intermediate 3;
(3) intermediate 3 is dissolved in 4N hydrogen chloride dioxane solution, reacts at room temperature 2h, reaction is finished, and solid, mistake is precipitated
Filter, obtains intermediate 4;
(4) intermediate M and DIEA are dissolved in n,N-Dimethylformamide, under condition of ice bath, EDCI and HOBt is added, after
After continuous stirring 1h, intermediate 4 is added, finishes, is stirred overnight at room temperature, reaction solution is poured into ice water by end of reaction, ethyl acetate
Three times, combined ethyl acetate is successively washed three times with water and saturated sodium chloride solution, and anhydrous sodium sulfate dries, filters for extraction, filter
Liquid evaporating solvent under reduced pressure, silica gel column chromatography obtain II-1~II-9 in formula (II) compound;
Further, II-1, II-7, II-9 in formula (II) compound are dissolved in methanol, the hydrogen chloride two of 4N is added
48h is stirred at room temperature in six ring solution of oxygen, and solid is precipitated, and filtering obtains II-10~II-12 in formula (II) compound.
Further, in one or more embodiments, the side of the preparation formula (II) compound or pharmaceutically acceptable salt thereof
Method is carried out according to reaction as follows:
Further, in one or more embodiments, the reagent and condition of each step in above-mentioned reaction route are as follows:
(a) NBS, DMF, r.t. (room temperature);(b) 1-Boc- piperazine, DIEA, DMF, 110 DEG C;(c) hydrogen chloride-dioxy six
Ring, methanol, r.t.;(m)(Boc)2O, NaOH (aq), THF, r.t.;(n) methanol, H2SO4, 60 DEG C;(o) NBS, AIBN, CCl4,
76.8℃;(p) replace secondary amine, DIEA, CH3CN, 80 DEG C;(q) ethyl alcohol, NaOH (aq, 10M), 80 DEG C;(d) EDCI, HOBt,
DIEA, DMF, r.t.;(l) hydrogen chloride-dioxane, methanol, r.t..
On the other hand, present invention also provides a kind of method for preparing compound or pharmaceutically acceptable salt thereof shown in formula (III), institutes
Stating method, reaction route (reaction route 2) carries out as described below:
Wherein, X is selected from H, F, Cl, Br;Y is C1-C8Linear or branched alkyl group;
Further, X is selected from H, F, Cl, Br;Y is C1-C5Linear or branched alkyl group;
Further, X H, Cl or Br;Y is methyl, ethyl, isopropyl or tert-butyl;
Further, which comprises
(i) it is dissolved in isopropanol with starting material 5, reacts to obtain intermediate 6a-6d with amine is replaced;
(ii) intermediate 6a-6d and 1-Boc- piperazine are in dioxane and K2CO3In the presence of reaction generate intermediate 7a-7d;
(iii) intermediate 7a-7d reacts under glacial acetic acid existence condition with NCS/NBS, obtains intermediate 7e-7l;
(iv) intermediate 7e-7l reacts in methanol solution with hydrogen chloride dioxane solution, takes off Boc protecting group, obtains
Intermediate 8a-8l;
(v) after intermediate 8a-8l reacts in the presence of EDCI, HOBt, DIEA and DMF with intermediate acid N, intermediate is obtained
9a-9l;
(vi) it by the methanol solution of intermediate 9a-9l, is reacted with the dioxane solution of hydrogen chloride, obtains formula (III) chemical combination
The hydrochloride of object;
Further, the intermediate acid N is
Further, in one or more more specifically embodiments, the preparation formula (III) compound or its can
The method of pharmaceutical salts includes:
(i) starting material 5 is suspended in isopropanol, is added under condition of ice bath and replaces amine, is finished, reacted at room temperature 2h, subtract
Solvent is evaporated off in pressure, and ethyl acetate is added to dissolve for residue and water, water phase are extracted with ethyl acetate three times, combined ethyl acetate, is saturated chlorine
Change sodium solution washing three times, anhydrous sodium sulfate dries, filters, evaporating solvent under reduced pressure, and short column of silica gel column chromatography obtains intermediate 6a-
6d;
(ii) intermediate 6a-6d and 1- tert-butoxycarbonyl-piperazine is dissolved in dioxane, addition Anhydrous potassium carbonate, 150
DEG C 1~2h of microwave reaction, reaction are finished, filtering, and filter cake methanol washing, merging filtrate, filtrate decompression is evaporated off solvent, obtains brown oil
Object, silica gel column chromatography obtain intermediate 7a-7d;
(iii) intermediate 7a-7d and NCS/NBS are dissolved in glacial acetic acid, react at room temperature 2h, and reaction is finished, and remove ice vinegar under reduced pressure
Acid is greater than 7 with 2N sodium hydrate regulator solution pH, is extracted with ethyl acetate three times, combined ethyl acetate, successively uses water and saturation
Sodium chloride solution washs three times, and anhydrous sodium sulfate dries, filters, and solvent is evaporated off in filtrate decompression, and silica gel column chromatography obtains intermediate
7e-7l;
(iv) intermediate 7e-7l is dissolved in methanol, 4N hydrogen chloride dioxane solution is added, is stirred at room temperature, reacted
24h;Reaction is finished, and white solid, filtering is precipitated, and a small amount of methanol washing of filter cake obtains intermediate 8a-8l;
(v) two (2- chloroethyl) amine hydrochlorate raw materials 15 and 10% sodium hydroxide solution are suspended in methylene chloride, ice
(Boc) is added dropwise under the conditions of bath2O is finished, and for 24 hours, reaction is finished, evaporating solvent under reduced pressure, silica gel column chromatography, colorless oil for room temperature reaction
Object obtains intermediate 16;
(vi) 4- chlorobenzene acetonitrile and intermediate 16 are dissolved in and are steamed in DMF again, under condition of ice bath, be slowly added to 40% hydrogenation
Sodium finishes, and reacts at room temperature 30min, 60 DEG C of reaction 18h, and reaction solution is poured into ice water by end of reaction, ethyl acetate extraction three
Secondary, combined ethyl acetate is successively washed three times with water and saturated sodium chloride solution, and anhydrous sodium sulfate dries, filters, filtrate decompression
Solvent, silica gel column chromatography is evaporated off, white solid obtains intermediate 17;
(vii) intermediate 17 being dissolved in ethyl alcohol, 10N sodium hydroxide solution, 80 DEG C of back flow reaction 48h is added, reaction is finished,
Remove ethyl alcohol under reduced pressure, with 1N hydrochloric acid solution tune pH less than 3, filtering obtains white light yellow complexion solid, is recrystallized with ethyl acetate/methanol,
White solid obtains intermediate N;
(viii) intermediate acid N and DIEA are dissolved in DMF, under condition of ice bath, EDCI, HOBt is added, stirs 1h, is added
12h is stirred at room temperature in intermediate 8a-8l, and reaction solution is poured into ice water by end of reaction, and ethyl acetate extracts three times, merges acetic acid
Ethyl ester is successively washed with water and saturated sodium chloride solution, and anhydrous sodium sulfate dries, filters, evaporating solvent under reduced pressure, silica gel column layer
Analysis, obtains intermediate 9a-9l;
(ix) intermediate 9a-9l is dissolved in methanol solution, the hydrogen chloride dioxane solution of 4N is added, is stirred at room temperature,
For 24 hours, reaction is finished for reaction, and solid, filtering is precipitated, and filter cake recrystallizing methanol obtains the hydrochloride of formula (III) compound.
Further, in one or more embodiments, the side of the preparation formula (III) compound or pharmaceutically acceptable salt thereof
Method is carried out according to reaction as follows:
Further, in one or more embodiments, the reagent and condition of each step in above-mentioned reaction route are as follows:
(e)YNH2, isopropanol, r.t. (room temperature);(f) 1-Boc- piperazine, K2CO3, dioxane, 150 DEG C;(g)NCS/
NBS, AcOH;2N NaOH;(h) hydrogen chloride-dioxane, methanol, r.t.;(r)(Boc)2O, CH2Cl2, 10%NaOH (aq),
r.t;(s) NaH, DMF, 60 DEG C;(t) ethyl alcohol, 10N NaOH (aq);(k) EDCI, HOBt, DIEA, DMF, r.t.;(j) chlorination
Hydrogen-dioxane, methanol, r.t..
In another aspect, it includes formula as described above (I) or formulas (II) or formula this application provides a kind of pharmaceutical composition
(III) compound shown in or its isomers or solvate or officinal salt.
Another aspect, this application provides compound shown in formula as described above (I) or formula (II) or formula (III) or its is different
Structure body or solvate or officinal salt, or include compound or its isomers shown in the formula (I) or formula (II) or formula (III)
Or the pharmaceutical composition of solvate or officinal salt is preparing the application in Akt inhibitor.
Another aspect, this application provides compound shown in formula as described above (I) or formula (II) or formula (III) or its is different
Structure body or solvate or officinal salt, or include compound or its isomers shown in the formula (I) or formula (II) or formula (III)
Or the pharmaceutical composition application in preparation of anti-tumor drugs of solvate or officinal salt;Further, the tumour is
Lymphoma mantle cell.
In another aspect, this application provides a kind of combinations of drug combination comprising as described above formula (I) or formula (II) or
Compound shown in formula (III) or its isomers or solvate or officinal salt, or include the formula (I) or formula (II) or formula
(III) pharmaceutical composition and anti-tumor drug of compound shown in or its isomers or solvate or officinal salt are swollen in treatment
The use in conjunction of tumor especially lymphoma mantle cell.
Specific embodiment
Combined with specific embodiments below, the application is further described.It should be understood that these embodiments are merely to illustrate the application
Rather than limitation scope of the present application.In the following examples, the experimental methods for specific conditions are not specified, usually according to conventional strip
Part or according to the normal condition proposed by manufacturer.
Unless otherwise defined, it anticipates known to all professional and scientific terms as used herein and one skilled in the art
Justice is identical.In addition, any method similar to or equal to what is recorded and material all can be applied in the application method.Wen Zhong
The preferred implement methods and materials are for illustrative purposes only.
The preparation of bromo- 7H- pyrrolo- [2,3-d] pyrimidine hydrochloride (intermediate 4) of embodiment 14- piperazine -5-
(1) preparation of chloro- 7H- pyrrolo- [2,3-d] pyrimidine (intermediate 2) of the bromo- 4- of 5-
4- chloropyrrolo [2,3-d (20mmol) is dissolved in 20ml DMF, is added NBS (21mmol), 12h is stirred at room temperature, is reacted
After, reaction solution is poured into 200ml ice water, is filtered, filter cake is washed with water, and it is dry, obtain intermediate 2.Pale solid,
Yield is 94.6%, Mp:290-292 DEG C.1H NMR(400MHz,DMSO-d6)δ(ppm):13.00(s,1H),8.64(s,1H),
7.97(s,1H).MS(ESI)m/z:232[M+H]+.
(2) preparation of bromo- 7H- pyrrolo- [2,3-d] pyrimidine (intermediate 3) of 4- (4-Boc-1- piperazine) -5-
By intermediate 2 (5mmol), 1- tert-butoxycarbonyl-piperazine (6mmol) and DIEA (7.5mmol) are dissolved in 5ml dioxy six
In ring, 20ml water is added in 80 DEG C of microwave reaction 2h, evaporating solvent under reduced pressure, and ethyl acetate extraction merges organic phase, successively uses
Three times, anhydrous sodium sulfate dries, filters, and silica gel column chromatography obtains crude product, with ethyl alcohol weight for 20ml water, saturated sodium chloride solution washing
Crystallization, obtains intermediate 3.White solid, yield 78.5%.1H NMR(400MHz,DMSO-d6)δ(ppm):12.21(s,1H),
8.37 (s, 1H), 7.52 (d, J=2.6Hz, 1H), 3.52 (s, 8H), 1.42 (s, 9H) .MS (ESI) m/z:382 [M+H]+.
(3) preparation of bromo- 7H- pyrrolo- [2,3-d] pyrimidine hydrochloride (intermediate 4) of 4- piperazine -5-
Intermediate 3 (3.5mmol) is dissolved in the 4N hydrogen chloride dioxane solution of 4ml, 2h is reacted at room temperature.End of reaction
Afterwards, there is solid precipitation, filter, obtain intermediate 4.White solid, yield 99.2%.MS(ESI)m/z:282[M+H]+。
The preparation of 2 intermediate M of embodiment
(1) 2- (t-butoxycarbonyl amino) -2- (4- chlorphenyl) acetic acid (intermediate M1) preparation
2- amino -2- (4- chlorphenyl) acetic acid (5mmol) is dissolved in tetrahydrofuran solution, 2N sodium hydroxide solution is added dropwise
It is greater than 8 to pH, at the uniform velocity dropwise addition (Boc)2The tetrahydrofuran solution (tetrahydrofuran/water=2:1, v/v) of O (7.5mmol).It finishes,
React at room temperature 3h.After completion of the reaction, pH is adjusted less than 2 with 1N hydrochloric acid solution, be extracted with ethyl acetate, merge organic phase, with
20mL saturated sodium chloride solution is washed three times, and anhydrous sodium sulfate dries, filters, evaporating solvent under reduced pressure, obtains intermediate M1, clean oil
Shape object, yield 71.3%.
(2) preparation of 2- (4- chlorphenyl) methyl acetate (intermediate 12)
Raw material 4- chlorobenzene acetic acid (intermediate 11,40mmol) is dissolved in 25ml methanol, the 5 drop concentrated sulfuric acids, back flow reaction is added
5h.Evaporating solvent under reduced pressure obtains grease.Be added 25ml ethyl acetate dissolution, successively use 25ml saturated sodium bicarbonate solution, water and
Saturated sodium chloride solution is washed three times, and anhydrous sodium sulfate dries, filters, and solvent is evaporated off in filtrate decompression, obtains intermediate 12, light yellow
Grease, yield 97.6%.1H NMR(400MHz,DMSO-d6) δ (ppm): 7.39 (d, J=8.4Hz, 2H), 7.30 (d, J
=8.4Hz, 2H), 3.70 (d, 2H), 3.61 (s, 3H) .MS (ESI) m/z:185 [M+H]+。
(3) preparation of the bromo- 4- chlorophenyl acetate (intermediate 13) of α-
Intermediate (12,27.95mmol) is dissolved in 20ml CCl4In, N- bromo-succinimide is added in 3h in three times
Solvent, silicon is evaporated off in (27.95mmol) and azodiisobutyronitrile (AIBN, 27.95mmol), back flow reaction 2h, filtering, filtrate decompression
Plastic column chromatography, elution system are petrol ether/ethyl acetate=100/1, obtain intermediate 13, light yellow oil, yield is
94.3%.1H NMR(400MHz,DMSO-d6) δ (ppm): 7.59 (d, J=8.4Hz, 2H), 7.49 (d, J=8.4Hz, 2H),
6.00(s,1H),3.73(s,3H).MS(ESI)m/z:263[M+H]+.
(4) method is led in the synthesis of alpha-substituted -4- chlorophenyl acetate (intermediate 14)
Intermediate 13 (2mmol) is dissolved in 5ml acetonitrile, is added and replaces secondary amine (2.2mmol) and DIEA (3mmol), reflux
React 4h.Reaction is finished, evaporating solvent under reduced pressure, and 20ml water is added, three times with the extraction of 20ml ethyl acetate, combined ethyl acetate,
Three times, anhydrous sodium sulfate dries, filters, and solvent, silica gel column layer is evaporated off in filtrate decompression for 20ml water and saturated sodium chloride solution washing
Analysis, elution system are petrol ether/ethyl acetate=30:1-15:1-8:1-4:1-1:1, obtain intermediate 14.
Intermediate 14a: methyl 2- (4- chlorphenyl) -2- (dimethylamino) acetic acid, yellow oil, yield 61.8%.1H NMR(400MHz,CDCl3) δ (ppm): 7.39 (d, J=8.8Hz, 2H), 7.33 (d, J=8.8Hz, 2H), 3.86 (s, 1H),
3.70(s,3H),2.24(s,6H).MS(ESI)m/z:228[M+H]+.
Intermediate 14b: methyl 2- (4- chlorphenyl) -2- (diethylin) acetic acid, yellow oil, yield 70.2%.1H NMR(400MHz,CDCl3) δ (ppm): 7.39 (d, J=8.4Hz, 2H), 7.31 (d, J=8.8Hz, 2H), 3.94 (s, 1H),
3.68(s,3H),2.36(q,4H),1.60(t,6H).MS(ESI)m/z:256[M+H]+.
Intermediate 14c: methyl 2- (4- chlorphenyl) -2- (pyrroles -1- base) acetic acid, colorless oil, yield 90%.1H
NMR(400MHz,CDCl3) δ (ppm): 7.43 (d, J=8.4Hz, 2H), 7.32 (d, J=8.4Hz, 2H), 3.90 (s, 1H),
3.68(s,3H),2.55-2.43(m,4H),1.82-1.81(m,4H).MS(ESI)m/z:254[M+H]+.
Intermediate 14d: methyl 2- (4- chlorphenyl) -2- (3,5- lupetidine -1- base) acetic acid, colorless oil are received
Rate is 65.7%.1H NMR(400MHz,CDCl3)δ(ppm):7.31-7.26(m,4H),4.45(s,1H),3.69(s,3H),
2.73-2.67 (m, 2H), 2.70-1.84 (m, 6H), 1.07 (t, J=6.0Hz, 6H) .MS (ESI) m/z:296 [M+H]+.
Intermediate 14e: methyl 2- (4- chlorphenyl) -2- morpholine acetic acid, colorless and transparent oily object, yield 71.4%.1H
NMR(400MHz,DMSO-d6) δ (ppm): 7.45 (d, J=9.2Hz, 2H), 7.43 (d, J=9.2Hz, 2H), 4.16 (s, 1H),
3.61 (s, 3H), 3.57 (d, J=4.4Hz, 4H), 2.35 (d, J=4.4Hz, 4H) .MS (ESI) m/z:270 [M+H]+.
Intermediate 14f: tert-butyl 4- (1- (4- chlorphenyl) -2- methoxyl group -2- ethyoxyl) piperazine -1- carboxylate, it is colourless
Transparent oil, yield 100%.1H NMR(400MHz,CDCl3) δ (ppm): 7.38 (d, J=8.4Hz, 2H), 7.33 (d, J
=8.4Hz, 2H), 3.99 (s, 1H), 3.69 (s, 3H), 3.44 (s, 4H), 2.39 (s, 4H), 1.44 (s, 9H) .MS (ESI) m/
z:369[M+H]+.
Intermediate 14g: methyl 2- (4- chlorphenyl) -2- (4- methyl piperazine base) acetic acid, brown oil, yield are
66.7%.1H NMR(400MHz,CDCl3) δ (ppm): 7.39 (d, J=8.4Hz, 2H), 7.32 (d, J=8.4Hz, 2H), 3.96
(s,1H),3.68(s,3H),2.63-2.40(m,8H),2.31(s,3H).MS(ESI)m/z:283[M+H]+.
Intermediate 14h: methyl 2- [4- (t-butoxycarbonyl amino) piperidin-1-yl] -2- (4- chlorphenyl) acetic acid, white are solid
Body, yield 70.6%.1H NMR(400MHz,CDCl3) δ (ppm): 7.37 (d, J=8.4Hz, 2H), 7.32 (d, J=
8.4Hz,2H),4.43(br,1H),3.96(s,1H),3.68(s,3H),3.49(br,1H),2.86(br,1H),2.67(br,
1H), 2.24 (t, J=10.8Hz, 1H), 2.01-1.84 (m, 3H), 1.45-1.43 (s, 10H) .MS (ESI) m/z:383 [M+H
]+.
(5) alpha-substituted -4- chlorobenzene acetic acid (intermediate M2-M9) synthesis lead to method
Intermediate 14 (1mmol) is suspended in 3ml ethanol/water (2/1, V/V), 1N sodium hydroxide solution 2ml, room temperature are added
Stir 4h.Reaction is finished, and removes ethyl alcohol under reduced pressure, and adjusting pH with 1N hydrochloric acid solution is about 6, and solid, filtering is precipitated, and filter cake is washed with water
It washs, obtains intermediate M2-M9。
Or: with 1N hydrochloric acid solution adjust pH be about 6 solid is not precipitated when, ethyl alcohol is evaporated off, is extracted with dichloromethane, merge two
Chloromethanes, evaporating solvent under reduced pressure obtain intermediate M2-M9。
Intermediate M2: 2- (4- chlorphenyl) -2- (dimethylamino) acetic acid, white solid, yield 81.5%.1H NMR
(400MHz,CDCl3) δ (ppm): 7.41 (d, J=7.2Hz, 2H), 7.16 (d, J=7.2Hz, 2H), 4.77 (s, 1H), 2.84
(s,6H).MS(ESI)m/z:212[M-H]-.
Intermediate M3: 2- (4- chlorphenyl) -2- (lignocaine) acetic acid, white solid, yield 20%.1H NMR
(400MHz, MeOD) δ 7.64-7.54 (m, 2H), 7.48-7.41 (m, 2H), 4.56 (s, 1H), 3.21 (td, J=13.3,
6.4Hz, 2H), 3.05 (s, 2H), 1.25 (t, J=7.1Hz, 6H) .MS (ESI) m/z:240 [M-H]-.
Intermediate M4: 2- (4- chlorphenyl) -2- (pyrroles -1- base) acetic acid, white solid, yield 86.9%.1H NMR
(400MHz,CD3OD) δ (ppm): 7.56 (d, J=8.8Hz, 2H), 7.46 (d, J=8.4Hz, 2H), 4.51 (s, 1H), 3.31-
3.29(m,4H),2.11-1.99(m,4H).MS(ESI)m/z:238[M-H]-.
Intermediate M5: 2- (4- chlorphenyl) -2- (3,5- lupetidine -1- base) acetic acid, white solid, yield are
58.8%.1H NMR(400MHz,DMSO-d6) δ (ppm): 7.43 (d, J=8.8Hz, 2H), 7.35 (d, J=8.8Hz, 2H),
3.81 (s, 1H), 3.09-3.07 (m, 1H), 2.56-2.54 (m, 1H), 1.70-1.63 (m, 4H), 1.51 (t, J=10.8Hz,
1H), 0.80 (d, J=5.2Hz, 3H), 0.70 (d, J=8.4Hz, 3H), 0.54-0.45 (m, 1H) .MS (ESI) m/z:280 [M-
H]-.
Intermediate M6: 2- (4- chlorphenyl) -2- morpholine acetic acid, white solid, yield 83.9%.1H NMR(400MHz,
CD3OD) δ (ppm): 7.55 (d, J=8.4Hz, 2H), 7.45 (d, J=8.8Hz, 2H), 4.41 (s, 1H), 3.88-3.81 (m,
3H),3.30-3.22(m,3H),2.88-2.85(m,2H).MS(ESI)m/z:254[M-H]-.
Intermediate M7: 2- (4- tert-butoxycarbonyl-piperazine base) -2- (4- chlorphenyl) acetic acid, white solid, yield are
43.4%.1H NMR(400MHz,DMSO-d6) δ (ppm): 7.45 (d, J=8.8Hz, 2H), 7.42 (d, J=8.8Hz, 2H),
4.05(s,1H),3.30-3.24(m,4H),2.37-2.29(m,4H),1.37(s,9H).MS(ESI)m/z:353[M-H]-.
Intermediate M8: 2- (4- chlorphenyl) -2- (4- methyl piperazine base) acetic acid, white light yellow complexion solid, yield 93.9%.1H NMR(400MHz,CD3OD) δ (ppm): 7.50 (d, J=8.4Hz, 2H), 7.34 (d, J=8.4Hz, 2H), 3.88 (s, 1H),
3.31-3.30(m,3H),3.14(s,3H),2.74(s,3H),2.65(br,2H).MS(ESI)m/z:267[M-H]-.
Intermediate M9: 2- [4- (t-butoxycarbonyl amino) piperidin-1-yl] -2- (4- chlorphenyl) acetic acid, white solid are received
Rate is 59.8%.1H NMR(400MHz,DMSO-d6) δ (ppm): 7.42 (s, 4H), 6.84 (d, J=7.2Hz, 1H), 4.04 (s,
1H), 3.26 (s, 1H), 3.05 (d, J=11.2Hz, 1H), 2.64 (d, J=11.6Hz, 1H), 2.36 (t, J=10.8Hz,
1H), 2.23 (t, J=10.8Hz, 1H), 1.75 (d, J=6.0Hz, 1H), 1.68 (d, J=12.4Hz, 1H), 1.50 (t, J=
12.0Hz,2H),1.36(s,9H).MS(ESI)m/z:367[M-H]-.
The preparation of 3 target compound II-1~II-12 of embodiment
(1) preparation of target compound II-1~II-9
Intermediate acid M (0.4mmol) and DIEA (2mmol) are dissolved in 2ml DMF, under condition of ice bath, EDCI is added
(0.48mmol) and HOBt (0.48mmol) continues after stirring 1h, is added intermediate 4 (0.4mmol).It finishes, was stirred at room temperature
Night.Reaction solution is poured into 20ml ice water by end of reaction, and 20ml ethyl acetate extracts three times, and combined ethyl acetate is successively used
Three times, anhydrous sodium sulfate dries, filters, and solvent, silica gel column layer is evaporated off in filtrate decompression for 20ml water and saturated sodium chloride solution washing
Analysis, elution system are ethyl acetate/methanol=100:1~60:1 or methylene chloride/methanol=50:1~30:1, obtain target product
II-1~II-9.
II-1: tert-butyl { 2- [4- (the bromo- 7H- pyrroles of 5- [2,3-d] pyrimidine-4-yl) piperazine -1- base] -1- (4- chlorobenzene
Base) -2- oxygen ethyl } carbamate, brown solid, yield 43.8%, Mp:128~131 DEG C.1H NMR(400MHz,MeOD)
δ(ppm):8.24(s,1H),7.39(s,4H),7.34(s,1H),5.67(s,1H),3.95–3.84(m,1H),3.84–3.72
(m, 2H), 3.72-3.64 (m, 1H), 3.64-3.53 (m, 2H), 3.53-3.42 (m, 1H), 3.31 (dt, J=3.2,1.6Hz,
3H),3.21–3.10(m,1H),1.43(s,9H).13C NMR(100MHz,CD3OD)δ(ppm):169.20,159.69,
155.87,151.33,150.39,136.03,133.96,129.35,128.79,123.95,105.14,86.58,79.51,
54.66,49.76,49.50,45.14,42.12,27.28.
II-2:1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (two
Methylamino) ethyl ketone, light tan solid, yield 74.4%, Mp:103~105 DEG C.1H NMR(400MHz,CDCl3)δ(ppm):
12.06 (s, 1H), 8.37 (s, 1H), 7.40 (d, J=8.5Hz, 2H), 7.34 (d, J=8.5Hz, 2H), 7.29 (s, 1H),
4.26(s,1H),3.95-3.91(m,1H),3.88–3.62(m,4H),3.59-3.50(m,2H),3.33–3.19(m,1H),
2.32 (s, 6H), 1.26 (t, J=7.1Hz, 1H)13C NMR(100MHz,CDCl3)δ(ppm):169.27,159.67,
151.95,150.63,134.55,134.21,130.33,129.00,123.49,105.36,87.34,71.55,50.38,
49.59,45.29,43.39,42.12.
II-3:1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (two
Ethylamino) ethyl ketone, light tan solid, yield 62.3%, Mp:83~87 DEG C.1H NMR(400MHz,CDCl3)δ11.78(s,
1H), 8.41 (s, 1H), 7.39 (d, J=8.3Hz, 2H), 7.34 (d, J=8.4Hz, 2H), 4.84 (s, 1H), 3.94-3.81
(m, 3H), 3.71-3.55 (m, 4H), 3.49-3.40 (m, 1H), 2.81 (dd, J=13.2,6.8Hz, 2H), 2.63 (dd, J=
13.1,6.7Hz, 2H), 1.28 (s, 2H), 1.03 (t, J=7.0Hz, 6H)13C NMR(100MHz,CDCl3)δ170.11(s),
159.73(s),151.91(s),150.50(s),135.28(s),133.74(s),130.66(s),128.68(s,2C),
123.50(s,2C),105.38(s),87.34(s),65.77(s),50.45(s),49.75(s),45.30(s),44.33(s,
C),41.90(s),29.71(s),13.04(s,2C).
II-4:1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (pyrrole
Cough up -1- base) ethyl ketone, brown solid, yield 64.6%.1H NMR(400MHz,CDCl3)δ(ppm):11.87(s,1H),8.36
(s, 1H), 7.38 (dd, J=42.1,7.4Hz, 4H), 4.37 (s, 1H), 3.71 (dd, J=98.1,45.4Hz, 7H), 3.26
(s, 1H), 2.61 (d, J=26.6Hz, 4H), 1.81 (s, 4H)13C NMR(100MHz,DMSO-d6)δ(ppm):168.76
(s),159.55(s),152.09(s),151.09(s),132.91(s),130.84(s),128.90(s,2C),124.84(s,
2C),104.96(s),86.24(s),67.78(s),51.74(s),50.30(s,2C),45.24(s,2C),42.02(s,2C),
23.44(s,2C),14.55(s).
II-5:1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (3,
5- lupetidine -1- base) ethyl ketone, brown solid, yield 51.0%, Mp:114~117 DEG C.1H NMR(400MHz,CDCl3)δ
(ppm): 11.85 (s, 1H), 8.38 (s, 1H), 7.38 (d, J=8.5Hz, 2H), 7.33 (d, J=8.5Hz, 2H), 4.39 (s,
1H), 3.95-3.71 (m, 4H), 3.70-3.47 (m, 3H), 3.47-3.33 (m, 1H), 2.85 (t, J=8.3Hz, 2H), 1.83-
1.62(m,4H),1.54-1.43(m,1H),1.25(s,2H),0.83-0.78(m,6H),0.55-0.47(m,1H).13C NMR
(100MHz,CDCl3)δ(ppm):169.38,159.70,151.92,150.65,133.82,130.54,128.72,123.23,
105.30,87.52,71.53,59.43,58.51,50.39,49.70,45.26,42.10,31.94,31.34,31.15,
29.71,29.38,22.71,19.61,14.15.
II-6:1- [4- (5- bromo- 7H- [2,3-d] pyrimidine-4-yl) piperazinyl] -2- (4- chlorphenyl) -2- morpholine ethyl ketone,
Light tan solid, yield 70.0%, Mp:110~114 DEG C.1H NMR(400MHz,CDCl3)δ(ppm):11.91(s,1H),
8.38 (s, 1H), 7.40 (d, J=8.5Hz, 2H), 7.35 (d, J=8.5Hz, 2H), 7.28 (s, 1H), 4.00-3.62 (m,
10H), 3.56 (dd, J=16.1,11.5Hz, 2H), 3.30 (dd, J=10.0,7.3Hz, 1H), 2.55 (s, 4H)13C NMR
(100MHz,CDCl3)δ(ppm):168.65,159.67,151.92,150.64,134.38,133.47,130.45,129.06,
123.33,105.36,87.45,71.15,66.89,60.43,51.75,50.38,49.58,45.30,42.15.
II-7: tert-butyl 4- { 2- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -1- (4- chlorobenzene
Base } -2- oxygen ethyl) piperazine -1- carboxylate, light tan solid, yield 76.2%, Mp:131~135 DEG C.1H NMR(400MHz,
CDCl3)δ(ppm):12.02(s,1H),8.30(s,1H),7.40–7.23(m,4H),7.20(s,1H),4.30(s,1H),
3.93–3.14(m,12H),2.58–2.28(m,4H),1.36(s,10H).
II-8:1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (4-
Methyl piperazine base) ethyl ketone, light tan solid, yield 51.6%, Mp:85~87 DEG C.1H NMR(400MHz,CDCl3)δ(ppm):
8.37 (s, 1H), 7.39 (d, J=8.5Hz, 2H), 7.33 (d, J=8.5Hz, 2H), 7.26 (s, 1H), 4.31 (s, 1H),
3.95-3.46 (m, 8H), 3.32 (dd, J=10.0,7.2Hz, 1H), 2.54 (d, J=26.6Hz, 7H), 2.28 (s, 3H)13C
NMR(100MHz,CDCl3)δ(ppm):168.87,159.67,151.96,150.68,134.12,133.92,130.37,
128.91,123.42,105.37,87.31,71.28,54.95,51.17,50.38,49.63,46.08,45.87,45.26,
42.19,10.76.
II-9: tert-butyl { { 1- { 2- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -1- (4- chlorine
Phenyl) -2- oxygen ethyl } piperidin-4-yl } methyl } carbamate, light tan solid, yield 54.5%, Mp:140~143 DEG C
。1H NMR(400MHz,CDCl3) δ (ppm): 11.63 (s, 1H), 8.36 (s, 1H), 7.37 (d, J=8.5Hz, 2H), 7.33 (d,
J=8.5Hz, 2H), 4.42 (d, J=52.5Hz, 2H), 3.93-3.40 (m, 9H), 3.32 (s, 1H), 3.00-2.75 (m, 2H),
2.32 (s, 1H), 2.19-1.99 (m, 2H), 1.91 (t, J=14.5Hz, 2H), 1.58-1.35 (m, 12H)
(2) preparation of target compound II-10~II-12
Target product II-1, II-7, II-9 are suspended in 2ml methanol solution, the dioxy six of 4N saturation hydrogen chloride is added
After reacting at room temperature 48h, white solid is precipitated in ring solution, and filtering obtains target product II-10~II-12.
II-10:2- amino -1- (4- (the bromo- 7H- pyrroles of 5- [2,3-d] pyrimidine-4-yl) piperazine -1- base) -2- (4- chlorobenzene)
Acetophenone hydrochloride, white solid, yield 72.5%, Mp:264~266 DEG C.1H NMR(400MHz,D2O)δ(ppm):8.08(s,
1H), 7.39 (d, J=8.6Hz, 2H), 7.35 (d, J=8.7Hz, 2H), 7.32 (s, 1H), 5.50 (s, 1H), 3.99-3.88
(m,1H),3.86–3.73(m,1H),3.71–3.47(m,5H),3.46–3.34(m,1H),3.02–2.90(m,1H).13C NMR
(100MHz,D2O)δ(ppm):166.38,154.28,146.67,143.18,136.26,130.14,129.94,129.51,
126.60,103.01,88.85,66.52,54.53,49.63,48.75,44.33,41.97.
II-11:1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (piperazine
Piperazine base) acetophenone hydrochloride, white solid, yield 98.9%.1H NMR(400MHz,D2O)δ(ppm):8.10(s,1H),7.43
(s, 5H), 7.35 (s, 1H), 5.54 (s, 1H), 4.05-3.94 (m, 1H), 3.83 (qd, J=12.9,4.5Hz, 2H), 3.76-
3.68(m,1H),3.67–3.30(m,15H),3.29–3.16(m,3H),2.93–2.82(m,1H).13C NMR(100MHz,
D2O)δ(ppm):164.96,154.30,146.52,143.05,137.33,131.14,130.53,126.65,125.98,
103.02,88.91,69.29,49.61,48.51,48.08,44.45,42.06,40.80.
II-12:2- [4- (amino methyl) piperidin-1-yl) -1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-)
Piperazinyl] -2- (4- chlorphenyl) acetophenone hydrochloride, white solid, yield 99.2%.1H NMR(400MHz,D2O)δ(ppm):
8.11(s,1H),7.45(s,5H),7.37(s,1H),5.52(s,1H),4.09–3.96(m,1H),3.97–3.28(m,14H),
3.26–2.81(m,6H),2.27-2.21(m,3H),2.05–1.76(m,3H).13C NMR(100MHz,D2O)δ(ppm):
164.76,154.54,151.00,146.71,143.36,137.35,130.49,130.42,126.57,125.95,103.14,
88.81,66.52,62.47,49.57,49.02,48.49,45.23,44.46,44.28,42.10.
The preparation of 4 intermediate 8 of embodiment
(1) preparation of the chloro- 6- substituted-amino pyrimidine (intermediate 6) of 4-
4,6- dichloro pyrimidine (5,30mmol) is suspended in 20ml isopropanol.It is added under condition of ice bath and replaces amine
(75mmol).It finishes, reacts at room temperature 2h.Evaporating solvent under reduced pressure, residue add the dissolution of 20ml ethyl acetate and 20ml water.Water phase is used
20ml ethyl acetate extracts three times, combined ethyl acetate, and 20ml saturated sodium chloride solution is washed three times, and anhydrous sodium sulfate is dry,
Filtering, evaporating solvent under reduced pressure, short column of silica gel column chromatography, elution system is petrol ether/ethyl acetate=5/1, obtains intermediate 6.
The chloro- 6- methylaminopyrimidin of intermediate 6a:4-, white solid, yield 88.0%, Mp:138~140 DEG C.1H NMR
(400MHz,DMSO-d6)δ(ppm):8.28(s,1H),7.68(s,1H),6.50(s,1H),2.82(s,3H).MS(ESI)m/
z:144[M-H]-.
The chloro- 6- ethylamino pyrimidine of intermediate 6b:4-, white solid, yield 81.4%, Mp:116~118 DEG C.1H NMR
(400MHz,DMSO-d6) δ (ppm): 8.25 (s, 1H), 7.71 (s, 1H), 6.47 (s, 1H), 3.14 (s, 2H), 1.13 (t, J=
7.2Hz,3H).MS(ESI)m/z:158[M+H]+.
The chloro- 6- isopropylamino pyrimidine of intermediate 6c:4-, white solid, yield 53.4%, Mp:78~80 DEG C.1H NMR
(400MHz,DMSO-d6) δ (ppm): 8.25 (s, 1H), 7.61 (s, 1H), 6.45 (s, 1H), 4.10 (s, 1H), 1.14 (d, J=
9.6Hz,6H).MS(ESI)m/z:172[M+H]+.
The tertiary fourth aminopyrimidine of the chloro- 6- of intermediate 6d:4-, white solid, yield 44.9%, Mp:126~128 DEG C.1H
NMR(400MHz,DMSO-d6)δ(ppm):8.26(s,1H),7.41(s,1H),6.53(s,1H),1.38(s,9H).MS(ESI)
m/z:186[M+H]+.
(2) preparation of 4- [4- (6- substituted-amino) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester (intermediate 7a-7d)
Intermediate 6 (15mmol) and 1- tert-butoxycarbonyl-piperazine (22.5mmol) are dissolved in 3ml dioxane, nothing is added
Aqueous carbonate potassium (4.15g, 30mmol), 150 DEG C of 1~2h of microwave reaction, reaction are finished, filtering, the washing of filter cake methanol, merging filtrate,
Solvent is evaporated off in filtrate decompression, obtains brown oil, silica gel column chromatography, and elution system is methylene chloride/methanol=10/1, obtains intermediate
Body 7a-7d.
Intermediate 7a:4- [4- (6- methylamino) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white light yellow complexion solid, yield
56.8%, Mp:191~192 DEG C.1H NMR(400MHz,DMSO-d6)δ(ppm):7.98(s,1H),6.68(s,1H),5.54
(s, 1H), 3.46-3.45 (m, 4H), 3.38-3.36 (m, 4H), 2.72 (d, J=4.8Hz, 3H), 1.41 (s, 9H) .MS (ESI)
m/z:294[M+H]+.
Intermediate 7b:4- [4- (6- ethylamino) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid, yield are
60.5%.Mp:182~185 DEG C.1H NMR(400MHz,DMSO-d6)δ(ppm):8.00(s,1H),6.70(s,1H),5.58
(s, 1H), 3.42-3.35 (m, 4H), 3.21-3.14 (m, 4H), 3.22-3.19 (m, 2H), 1.32 (s, 9H), 1.11 (t, J=
7.2Hz,3H).MS(ESI)m/z:308[M+H]+.
Intermediate 7c:4- [4- (6- isopropylamino) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white light yellow complexion solid are received
Rate is 73.6%, Mp:180~182 DEG C.1H NMR(400MHz,CDCl3)δ(ppm):8.14(s,1H),5.37(s,1H),4.73
(d, J=7.6Hz, 1H), 3.84-3.76 (m, 1H), 3.54-3.52 (m, 8H), 1.48 (s, 9H), 1.23 (d, J=6.4Hz,
6H).MS(ESI)m/z:322[M+H]+.
Intermediate 7d:4- [4- (6- tert-butylamino) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, off-white powder, yield
For 80%, Mp:171~176 DEG C.1H NMR(400MHz,DMSO-d6)δ(ppm):8.02(s,1H),6.41(s,1H),5.66
(s,1H),3.32(s,3H),2.51-2.49(m,5H),1.41(s,9H),1.35(s,9H).MS(ESI)m/z:336[M+H]+.
(3) system of 4- [4- (halogenated -6- substituted-amino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester (intermediate 7e-7l)
It is standby
Intermediate 7a-7d (0.4mmol) and NCS/NBS, (0.48mmol) are dissolved in 3ml glacial acetic acid, react at room temperature 2h.Instead
It should finish, remove glacial acetic acid under reduced pressure, be greater than 7 with 2N sodium hydrate regulator solution pH, three times with the extraction of 30ml ethyl acetate, merge second
Acetoacetic ester is successively washed three times with 30ml water and saturated sodium chloride solution, and anhydrous sodium sulfate dries, filters, and filtrate decompression is evaporated off
Solvent, silica gel column chromatography, eluant, eluent be petrol ether/ethyl acetate=3/1~5/1~10/1, methylene chloride/methanol=3/1~
30/1, obtain intermediate 7e-7i.Intermediate 7e-7i is direct plungeed into without structural identification to react in next step.
Intermediate 7e:4- [4- (the chloro- 6- methylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid, yield
It is 71.7%;
Intermediate 7f:4- [4- (the chloro- 6- ethylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid, yield
It is 82.3%;
Intermediate 7g:4- [4- (the chloro- 6- isopropylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white light yellow complexion are solid
Body, yield 66.0%;
Intermediate 7h:4- [4- (the chloro- 6- tert-butylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid,
Yield is 89.2%;
Intermediate 7i:4- [4- (the bromo- 6- methylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid, yield
It is 71.7%;
Intermediate 7j:4- [4- (the bromo- 6- ethylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid, yield
It is 88.1%;
Intermediate 7k:4- [4- (the bromo- 6- isopropylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white light yellow complexion are solid
Body, yield 85.0%;
Intermediate 7l:4- [4- (the bromo- 6- tert-butylamino of 5-) pyrimidine radicals]-piperazine -1- carboxylic acid tert-butyl ester, white solid,
Yield is 53.7%.
(4) preparation of 4- substituted pyrimidyl piperazine hydrochloride (intermediate 8)
Intermediate 7 (1mmol) is dissolved in 1ml methanol, 4N hydrogen chloride dioxane solution 4ml is added, is stirred at room temperature, instead
It should for 24 hours.Reaction is finished, and white solid, filtering is precipitated, and a small amount of methanol washing of filter cake obtains intermediate 8.
Intermediate 8a:4- (6- methylamino) pyrimidylpiperazine hydrochloride, white solid, yield 87.8%, Mp:270~
273℃。1H NMR(400MHz,D2O) δ (ppm): 8.10 (s, 1H), 6.73 (s, 1H), 3.93 (t, J=4.8Hz, 4H), 3.31
(t, J=4.8Hz, 4H), 2.83 (s, 3H) .MS (ESI) m/z:194 [M+H]+.
Intermediate 8b:4- (6- ethylamino) pyrimidylpiperazine hydrochloride, white solid, yield 96.4%, Mp:292~
296 DEG C, yield 67.6%.1H NMR(400MHz,D2O) δ (ppm): 8.08 (s, 1H), 5.72 (s, 1H), 3.91 (t, J=
4.8Hz, 4H), 3.29 (t, J=4.8Hz, 4H), 3.25 (q, J=7.2Hz, 2H), 1.15 (t, J=7.2Hz, 3H) .MS (ESI)
m/z:208[M+H]+.
Intermediate 8c:4- (6- isopropylamino) pyrimidylpiperazine hydrochloride, light tan solid, yield 93.6%, Mp:
260~265 DEG C, yield 66.4%.1H NMR(400MHz,D2O)δ(ppm):8.07(s,1H),5.71(s,1H),3.89(t,J
=4.8Hz, 4H), 3.77 (m, J=6.4Hz, 1H), 3.29 (t, J=4.8Hz, 4H), 1.16 (t, J=6.4Hz, 6H) .MS
(ESI)m/z:222[M+H]+.
Intermediate 8d:4- (6- tert-butylamino) pyrimidylpiperazine hydrochloride, white light yellow complexion solid, yield 94.8%,
Mp:305~310 DEG C, yield 81.8%.1H NMR(400MHz,D2O)δ(ppm):8.08(s,1H),5.73(s,1H),3.90
(t, J=5.2Hz, 4H), 3.30 (t, J=5.2Hz, 4H), 1.33 (s, 9H) .MS (ESI) m/z:236 [M+H]+.
Intermediate 8e:4- (the chloro- 6- methylamino of 5-) pyrimidylpiperazine hydrochloride, white solid, yield 99.0%, Mp:
235~239 DEG C, yield 71.9%.1H NMR(400MHz,D2O) δ (ppm): 8.14 (s, 1H), 3.88 (t, J=4.8Hz, 4H),
3.33 (t, J=4.8Hz, 4H), 2.96 (s, 3H) .MS (ESI) m/z:228 [M+H]+.
Intermediate 8f:4- (the chloro- 6- ethylamino of 5-) pyrimidylpiperazine hydrochloride, white solid, yield 84.1%, Mp:
223~226 DEG C, yield 87.9%.1H NMR(400MHz,D2O) δ (ppm): 8.12 (s, 1H), 3.86 (t, J=4.8Hz, 4H),
3.43 (q, J=7.2Hz, 2H), 3.33 (t, J=4.8Hz, 4H), 1.16 (t, J=7.2Hz, 3H) .MS (ESI) m/z:242 [M+
H]+.
Intermediate 8g:4- (the chloro- 6- isopropylamino of 5-) pyrimidylpiperazine hydrochloride, white solid, yield 94.6%,
Mp:196~199 DEG C, yield 69.2%.1H NMR(400MHz,D2O) δ (ppm): 8.10 (s, 1H), 4.04 (m, J=6.4Hz,
1H), 3.82 (t, J=4.8Hz, 4H), 3.33 (t, J=4.8Hz, 4H), 1.19 (t, J=6.4Hz, 6H) .MS (ESI) m/z:
256[M+H]+.
Intermediate 8h:4- (the chloro- 6- tert-butylamino of 5-) pyrimidylpiperazine hydrochloride, white solid, yield 95.8%,
Mp:230~233 DEG C, yield 59.5%.1H NMR(400MHz,D2O) δ (ppm): 8.08 (s, 1H), 3.66 (t, J=4.8Hz,
4H), 3.30 (t, J=5.2Hz, 4H), 1.35 (s, 9H) .MS (ESI) m/z:270 [M+H]+.
Intermediate 8i:4- (the bromo- 6- methylamino of 5-) pyrimidylpiperazine hydrochloride, white solid, yield 91%, Mp:255
~260 DEG C, yield 81.2%.1H NMR(400MHz,D2O) δ (ppm): 8.13 (s, 1H), 3.85 (t, J=5.2Hz, 4H),
3.33 (t, J=5.2Hz, 4H), 2.95 (s, 3H) .MS (ESI) m/z:272 [M+H]+.
Intermediate 8j:4- (the bromo- 6- ethylamino of 5-) pyrimidylpiperazine hydrochloride, white solid, yield 61.5%, Mp:
295~300 DEG C, yield 51.6%,1H NMR(400MHz,D2O) δ (ppm): 8.12 (s, 1H), 3.86 (t, J=5.2Hz, 4H),
3.43 (q, J=7.2Hz, 2H), 3.33 (t, J=5.2Hz, 4H), 1.16 (t, J=7.2Hz, 3H) .MS (ESI) m/z:286 [M+
H]+.
Intermediate 8k:4- (the bromo- 6- isopropylamino of 5-) pyrimidylpiperazine hydrochloride, white light yellow complexion solid, yield are
84.2%, Mp:255~260 DEG C, yield 78.8%.1H NMR(400MHz,D2O) δ (ppm): 8.13 (s, 1H), 4.04 (m, J=
6.4Hz, 1H), 3.88 (t, J=4.8Hz, 4H), 3.34 (t, J=4.8Hz, 4H), 1.21 (t, J=6.4Hz, 6H) .MS (ESI)
m/z:300[M+H]+.
Intermediate 8l:4- (the bromo- 6- tert-butylamino of 5-) pyrimidylpiperazine hydrochloride, light yellow solid, yield 97.3%,
Mp:185~188 DEG C, yield 78.7%.1H NMR(400MHz,D2O) δ (ppm): 8.15 (s, 1H), 3.74 (t, J=4.8Hz,
4H), 3.35 (t, J=5.2Hz, 4H), 1.40 (s, 9H) .MS (ESI) m/z:314 [M+H]+.
The preparation of 5 intermediate N of embodiment
(1) preparation of (2- chloroethyl) carbamate of tert-butyl two (intermediate 16)
Two (2- chloroethyl) amine hydrochlorates (15,73.5mmol) and 10% sodium hydroxide solution (161.7mmol) are suspended
In methylene chloride.(Boc) is added dropwise under condition of ice bath2O(66.8mmol).It finishes, room temperature reaction is for 24 hours.Reaction is finished, and is removed under reduced pressure
Solvent, silica gel column chromatography, elution system are petrol ether/ethyl acetate=20/1, obtain colorless oil intermediate 16, yield is
96.4%.1H NMR(400MHz,DMSO-d6) δ (ppm): 3.71-3.66 (m, 4H), 3.54 (t, J=6.4Hz, 4H), 1.40
(s,9H).MS(ESI)m/z:242[M+H]+.
(2) preparation of tert-butyl 4- (4- chlorphenyl) -4- cyano piperidine -1- carboxylate (intermediate 17)
4- chlorobenzene acetonitrile (10mmol) and intermediate 16 (11mmol) are dissolved in 5ml and steamed in DMF again, under condition of ice bath, is delayed
Slow that 40% sodium hydride (30mmol) is added, 1h is finished, and reacts at room temperature 30min, 60 DEG C of reaction 18h.End of reaction, by reaction solution
It is poured into 50ml ice water, 50ml ethyl acetate extracts three times, and combined ethyl acetate successively uses 50ml water and saturated sodium chloride solution
Three times, anhydrous sodium sulfate dries, filters for washing, and solvent, silica gel column chromatography is evaporated off in filtrate decompression, and elution system is petroleum ether/second
Acetoacetic ester=15:1 obtains white solid intermediate 17, yield 66.7%, Mp:102~105 DEG C.1H NMR(400MHz,DMSO-
d6) δ (ppm): 7.59 (d, J=8.8Hz, 2H), 7.52 (d, J=8.8Hz, 2H), 4.14-4.11 (d, J=12.4Hz, 2H),
3.01 (s, 2H), 2.13 (d, J=12.4Hz, 2H), 1.95 (td, J1=12.8Hz, J2=4.0Hz, 2H), 1.42 (s, 9H) .MS
(ESI)m/z:321[M+H]+.
(3) preparation of 1- (carbonyl tertbutyloxycarbonyl) -4- (4- chlorphenyl) piperidines -4- carboxylic acid (intermediate N)
Intermediate 17 (7.5mmol) is dissolved in 20ml ethyl alcohol, is added 10N sodium hydroxide solution (225mmol), 80 DEG C are returned
Stream reaction 48h.Reaction is finished, and removes ethyl alcohol under reduced pressure, and with 1N hydrochloric acid solution tune pH less than 3, filtering obtains white light yellow complexion solid, uses second
Acetoacetic ester/recrystallizing methanol obtains white solid intermediate N, yield 74.5%, Mp:173~176 DEG C.1H NMR(400MHz,
DMSO-d6) δ (ppm): 12.66 (s, 1H), 7.41 (s, 4H), 3.79 (d, J=13.6Hz, 2H), 2.96 (s, 2H), 2.35 (d,
J=13.2Hz, 2H), 1.74-1.66 (m, 2H), 1.39 (s, 9H) .MS (ESI) m/z:338 [M-H]-.
The preparation of 6 target compound III-1~III-12 of embodiment
(1) tert-butyl 4- { 4- [5- halogenated -6- (substituted-amino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorphenyl)
Method is led in the synthesis of piperidines -1- carboxylate (intermediate 9)
Intermediate acid N (0.5mmol) and DIEA (2.5mmol) are dissolved in 2ml DMF, under condition of ice bath, EDCI is added
(0.6mmol), HOBt (0.6mmol) stir 1h, are added intermediate 8a-l (0.5mmol), 12h is stirred at room temperature.End of reaction,
Reaction solution is poured into 20ml ice water, 20ml ethyl acetate extracts three times, combined ethyl acetate, successively with 20ml water and saturation chlorine
Change sodium solution washing, anhydrous sodium sulfate dries, filters, evaporating solvent under reduced pressure, silica gel column chromatography, and elution system is petroleum ether/second
Acetoacetic ester=8:1~2:1 obtains intermediate 9.
Intermediate 9a: tert-butyl 4- (4- chlorphenyl) -4- { 4- [6- (methylamino) pyrimidine-4-yl] piperazine -1- carbonyl } piperazine
Pyridine -1- carboxylate, white solid, yield 72.5%.1H NMR(400MHz,CDCl3)δ(ppm):8.05(s,1H),7.37–
7.32 (m, 2H), 7.24-7.18 (m, 2H), 5.66 (br, 1H), 5.26 (s, 1H), 3.99 (d, J=52.5Hz, 2H), 3.21
(d, J=75.1Hz, 10H), 2.86 (d, J=5.0Hz, 3H), 2.27 (d, J=13.0Hz, 2H), 1.87 (d, J=80.2Hz,
2H),1.45(s,8H),1.45(s,1H).
Intermediate 9b: tert-butyl 4- (4- chlorphenyl) -4- { 4- [6- (ethylamino-) pyrimidine-4-yl] piperazine -1- carbonyl } piperazine
Pyridine -1- carboxylate, pinkish solid, yield 67.6%.1H NMR(400MHz,CDCl3)δ(ppm):8.06(s,1H),
7.34 (d, J=8.6Hz, 2H), 7.21 (d, J=8.6Hz, 2H), 5.30 (s, 1H), 5.27 (s, 1H), 3.99 (d, J=
55.4Hz, 3H), 3.48-3.04 (m, 10H), 2.27 (d, J=13.1Hz, 2H), 1.86 (d, J=85.3Hz, 2H), 1.45 (s,
9H), 1.25 (t, J=7.2Hz, 3H)
Intermediate 9c: tert-butyl 4- (4- chlorphenyl) -4- { 4- [6- (isopropylamine) pyrimidine-4-yl] piperazine -1- carbonyl }
Piperidines -1- carboxylate, light tan solid, yield 66.4%.1H NMR(400MHz,CDCl3)δ(ppm):8.08(s,1H),
7.34 (d, J=8.6Hz, 2H), 7.20 (d, J=8.6Hz, 2H), 5.27 (s, 1H), 4.63 (d, J=6.8Hz, 1H), 3.99
(d, J=56.6Hz, 2H), 3.77 (dt, J=12.6,6.6Hz, 1H), 3.20 (d, J=66.2Hz, 8H), 2.27 (d, J=
13.0Hz, 2H), 1.86 (d, J=88.5Hz, 4H), 1.45 (s, 9H), 1.21 (d, J=6.4Hz, 6H)
Intermediate 9d: tert-butyl 4- { 4- [6- (tert-butylamino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorobenzene
Base) piperidines -1- carboxylate, white light yellow complexion solid, yield 81.8%.1H NMR(400MHz,DMSO-d6)δ7.97(s,1H),
7.44 (d, J=8.5Hz, 2H), 7.30 (d, J=8.5Hz, 2H), 6.37 (s, 1H), 5.55 (s, 1H), 3.81 (d, J=
12.2Hz, 2H), 3.08 (s, 8H), 2.21 (d, J=13.3Hz, 2H), 1.83-1.72 (m, 2H), 1.39 (s, 9H), 1.33 (s,
9H).
Intermediate 9e: tert-butyl 4- { 4- [5- chloro- 6- (methylamino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorobenzene
Base) piperidines -1- carboxylate, white solid, 71.9%.1H NMR(400MHz,CDCl3)δ(ppm):8.18(s,1H),7.34(d,
J=8.6Hz, 2H), 7.20 (d, J=8.7Hz, 2H), 5.34 (s, 1H), 5.30 (s, 1H), 3.99 (d, J=58.1Hz, 2H),
3.27 (s, 8H), 3.05 (d, J=4.8Hz, 3H), 2.27 (d, J=13.0Hz, 2H), 1.85 (d, J=81.1Hz, 3H), 1.45
(s,9H).
Intermediate 9f: tert-butyl 4- { 4- [5- chloro- 6- (ethylamino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorobenzene
Base) piperidines -1- carboxylate, white solid, yield 87.9%.1H NMR(400MHz,CDCl3)δ(ppm):8.15(s,1H),
7.34 (d, J=8.6Hz, 2H), 7.20 (d, J=8.6Hz, 2H), 5.24 (s, 1H), 3.97 (d, J=52.5Hz, 2H), 3.54-
3.46 (m, 2H), 3.22 (d, J=53.9Hz, 8H), 2.27 (d, J=13.1Hz, 2H), 1.86 (d, J=83.5Hz, 2H),
1.57 (s, 2H), 1.41 (s, 9H), 1.24 (t, J=7.2Hz, 3H)
Intermediate 9g: tert-butyl 4- { 4- [5- chloro- 6- (isopropylamine) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorine
Phenyl) piperidines -1- carboxylate, yellowish solid, yield 68.8%.1H NMR(400MHz,CDCl3)δ(ppm):8.14(s,
1H), 7.34 (d, J=8.6Hz, 2H), 7.20 (d, J=8.6Hz, 2H), 5.06 (d, J=7.7Hz, 1H), 4.32-4.21 (m,
1H), 3.99 (d, J=65.1Hz, 3H), 3.21 (d, J=60.0Hz, 8H), 2.26 (d, J=13.1Hz, 2H), 1.85 (d, J=
87.5Hz, 3H), 1.45 (s, 9H), 1.24 (d, J=6.5Hz, 6H)
Intermediate 9h: tert-butyl 4- { 4- [6- (tert-butylamino) -5- chlorine pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4-
Chlorphenyl) piperidines -1- carboxylate, yellowish solid, yield 59.5%.1H NMR(400MHz,CDCl3)δ(ppm):8.13
(s, 1H), 7.33 (d, J=8.6Hz, 2H), 7.20 (d, J=8.6Hz, 2H), 5.25 (s, 1H), 3.98 (d, J=62.5Hz,
2H), 3.20 (d, J=67.3Hz, 8H), 2.26 (d, J=12.8Hz, 2H), 1.85 (d, J=86.7Hz, 4H), 1.47 (d, J=
7.1Hz,9H),1.45(s,9H).
Intermediate 9i: tert-butyl 4- { 4- [5- bromo- 6- (methylamino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorobenzene
Base) piperidines -1- carboxylate, white solid, yield 48.8%.1H NMR(400MHz,CDCl3)δ(ppm):8.20(s,1H),
7.34 (d, J=8.6Hz, 2H), 7.20 (d, J=8.6Hz, 2H), 5.42 (s, 1H), 3.98 (d, J=54.4Hz, 3H), 3.27
(s, 8H), 3.09 (d, J=4.5Hz, 3H), 2.27 (d, J=13.5Hz, 2H), 1.85 (d, J=78.3Hz, 3H), 1.45 (s,
9H).
Intermediate 9j: tert-butyl 4- { 4- [5- bromo- 6- (ethylamino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4- chlorobenzene
Base) piperidines -1- carboxylate, white solid, yield 51.6%.1H NMR(400MHz,CDCl3)δ(ppm):8.15(s,1H),
7.34 (d, J=8.6Hz, 2H), 7.20 (d, J=8.7Hz, 2H), 5.25 (s, 1H), 3.98 (d, J=57.5Hz, 3H), 3.50
(dt, J=12.8,6.5Hz, 2H), 3.21 (d, J=74.9Hz, 8H), 2.27 (d, J=13.0Hz, 2H), 1.84 (d, J=
89.7Hz, 3H), 1.45 (s, 9H), 1.24 (t, J=7.2Hz, 3H)
Intermediate 9k: tert-butyl 4- (4- (5- bromo- 6- (isopropylamine) pyrimidine-4-yl) piperazine -1- carbonyl) -4- (4- chlorine
Phenyl) piperidines -1- carboxylate, white light yellow complexion solid, yield 78.8%.1H NMR(400MHz,CDCl3)δ(ppm):8.14
(s, 1H), 7.34 (d, J=8.6Hz, 2H), 7.20 (d, J=8.7Hz, 2H), 5.06 (d, J=7.7Hz, 1H), 4.31-4.20
(m, 1H), 3.99 (d, J=62.9Hz, 2H), 3.20 (d, J=64.0Hz, 10H), 2.27 (d, J=13.0Hz, 2H), 1.85
(d, J=78.8Hz, 2H), 1.45 (s, 9H), 1.24 (d, J=6.5Hz, 6H)
Intermediate 9l: tert-butyl 4- { 4- [5- bromo- 6- (tert-butylamino) pyrimidine-4-yl] piperazine -1- carbonyl } -4- (4-
Chlorphenyl) piperidines -1- carboxylate, light yellow solid, yield 78.7%.1H NMR(400MHz,CDCl3)δ(ppm):8.12
(s, 1H), 7.33 (d, J=8.6Hz, 2H), 7.20 (d, J=8.6Hz, 2H), 5.21 (s, 1H), 3.99 (d, J=59.2Hz,
2H), 3.22 (d, J=66.9Hz, 8H), 2.26 (d, J=13.1Hz, 2H), 2.04-1.57 (m, 4H), 1.46 (s, 9H), 1.45
(s,9H).
(2) preparation of target compound III-1~III-12
Intermediate 9a-9l (1mmol) is dissolved in 1mL methanol solution, the hydrogen chloride dioxane solution 4ml of 4N is added,
It is stirred at room temperature, reaction is for 24 hours.Reaction is finished, and solid, filtering is precipitated, and filter cake recrystallizing methanol obtains target product III.
III-1:[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (methylamino) pyrimidine-4-yl] piperazinyl } ketone salt
Hydrochlorate, white solid, yield: 72.2%, Mp:220~223 DEG C.1H NMR(400MHz,D2O)δ(ppm):7.93(s,1H),
7.31 (d, J=8.6Hz, 2H), 7.19 (d, J=8.7Hz, 2H), 5.35 (s, 1H), 3.68-3.53 (m, 4H), 3.51 (s,
2H), 3.34-3.32 (m, 2H), 3.25 (br, 2H), 3.17 (t, J=12.0Hz, 2H), 3.02 (br, 2H), 2.73 (s, 3H),
2.43 (d, J=14.5Hz, 2H), 2.12-2.01 (m, 2H)13C NMR(100MHz,D2O)δ(ppm):173.28(s),
159.43(s),154.51(s),148.25(s),140.25(s),133.15(s),129.45(s,2C),126.77(s,2C),
62.44(s),47.68(s,2C),41.41(s,2C),31.47(s,2C),27.74(s),20.35(s).
III-2:[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (ethylamino) pyrimidine-4-yl] piperazinyl } ketone hydrochloric acid
Salt, white solid, yield: 81.3%, Mp:193~198 DEG C.1H NMR(400MHz,D2O)δ(ppm):7.92(s,1H),7.30
(d, J=8.6Hz, 2H), 7.18 (d, J=8.6Hz, 2H), 5.36 (s, 1H), 3.65-3.48 (m, 10H), 3.33 (d, J=
13.3Hz, 3H), 3.15-3.09 (m, 3H), 3.01 (s, 2H), 2.43 (d, J=14.5Hz, 2H), 2.07 (t, J=13.4Hz,
2H), 1.07 (t, J=7.3Hz, 3H)13C NMR(100MHz,D2O)δ(ppm):173.24(s),148.28(s),140.30
(s),133.12(s),129.45(s,2C),126.78(s,2C),66.50(s,3C),62.45(s),47.69(s 2C),
41.43(s,2C),36.56(s,2C),31.49(s),12.71(s,2C).
III-3:[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (isopropylamine) pyrimidine-4-yl] piperazinyl } ketone salt
Hydrochlorate, white solid, yield: 98.0%, Mp:273~275 DEG C.1H NMR(400MHz,D2O)δ(ppm):7.97(s,1H),
7.36 (d, J=8.5Hz, 2H), 7.24 (d, J=8.6Hz, 2H), 5.42 (s, 1H), 3.75-3.58 (m, 9H), 3.38 (d, J=
13.3Hz, 2H), 3.22 (t, J=12.2Hz, 2H), 3.08 (s, 2H), 2.48 (d, J=14.6Hz, 2H), 2.19-2.07 (m,
2H), 1.14 (d, J=6.4Hz, 6H)13C NMR(100MHz,DMSO-d6)δ(ppm):171.20(s),142.50(s),
132.36(s),129.82(s,2C),127.47(s,2C),63.28(s),55.40(s),48.05(s,2C),43.63(s,
2C),41.43(s,2C),32.10(s),22.42(s,2C).
III-4:4- [6- (tert-butylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone salt
Hydrochlorate, white solid, yield: 72.6%, Mp:277~278 DEG C.1H NMR(400MHz,D2O)δ7.94(s,1H),7.32(d,J
=8.7Hz, 2H), 7.21 (d, J=8.7Hz, 2H), 5.42 (s, 1H), 3.62 (m, 4H), 3.37-3.33 (m, 3H), 3.27
(br, 2H), 3.19 (t, J=11.8Hz, 3H), 3.05 (br, 2H), 2.45 (d, J=14.4Hz, 2H), 2.15-2.04 (m,
2H),1.29(s,9H).13C NMR(100MHz,D2O)δ173.30(s),148.61(s),140.29(s),133.16(s),
129.46(s,2C),126.81(s,2C),80.63(s),66.52(s),52.06(s,2C),47.72(s,2C),41.45(s,
2C),31.49(s),27.69(s,4C).
III-5:{ 4- [5- chloro- 6- (methylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] first
Keto hydrochloride, white light yellow complexion solid, yield: 61.9%, Mp:204~208 DEG C.1H NMR(400MHz,D2O)δ(ppm):7.97
(s, 1H), 7.32 (d, J=8.6Hz, 2H), 7.19 (d, J=8.6Hz, 2H), 3.59 (d, J=14.9Hz, 8H), 3.33 (d, J
=13.3Hz, 2H), 3.26-3.13 (m, 4H), 2.99 (s, 2H), 2.89 (s, 3H), 2.42 (d, J=14.5Hz, 2H), 2.08
(t, J=11.8Hz, 2H)13C NMR(100MHz,D2O)δ(ppm):173.13(s),155.51(s),155.00(s),
146.31(s),140.45(s),133.13(s),129.50(s,2C),126.78(s,2C),94.10(s),66.50(s,3C),
62.45(s),47.68(s,2C),41.42(s,2C),31.57(s),28.36(s,2C).
III-6:{ 4- [5- chloro- 6- (ethylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] ketone
Hydrochloride, yellowish solid, yield: 85.0%, Mp:259~261 DEG C.1H NMR(400MHz,D2O)δ8.04(s,1H),7.39
(d, J=8.6Hz, 2H), 7.27 (d, J=8.6Hz, 2H), 3.74-3.62 (m, 7H), 3.45-3.38 (m, 4H), 3.30-3.22
(m, 3H), 3.06 (s, 2H), 2.50 (d, J=14.5Hz, 2H), 2.21-2.10 (m, 2H), 1.17 (t, J=7.2Hz, 3H)13C
NMR(100MHz,D2O)δ(ppm):173.12(s),155.39(s),154.35(s),146.25(s),140.48(s),
133.12(s),129.49(s,2C),126.79(s,2C),94.02(s),66.51(s,3C),47.69(s,2C),41.43(s,
2C),37.18(s,2C),31.59(s),13.31(s,C).
III-7:{ 4- [5- chloro- 6- (isopropylamine) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] first
Keto hydrochloride, white solid, yield: 76.2%, Mp:189~193 DEG C.1H NMR(400MHz,D2O)δ(ppm):8.01(s,
1H), 7.38 (d, J=8.5Hz, 2H), 7.24 (d, J=8.6Hz, 2H), 4.01 (dt, J=13.0,6.5Hz, 1H), 3.63 (d,
J=27.5Hz, 8H), 3.38 (d, J=13.3Hz, 2H), 3.26-3.20 (m, 2H), 3.02 (s, 2H), 2.47 (d, J=
14.5Hz, 2H), 2.18-2.07 (m, 2H), 1.19 (d, J=6.5Hz, 6H)13C NMR(100MHz,DMSO-d6)δ(ppm):
171.00(s),157.80(s),152.91(s),142.63(s),132.29(s),129.76(s,2C),127.45(s,2C),
97.11(s),66.83(s,2C),48.02(s,2C),43.39(s,2C),41.47(s,2C),32.22(s),22.57(s,
2C).
III-8:{ 4- [6- (tert-butylamino) -5- chlorine pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl]
Methanone hvdrochloric acid salt, white solid, yield: 75.1%, Mp:185~187 DEG C.1H NMR(400MHz,D2O)δ8.08(s,1H),
7.42 (d, J=8.5Hz, 2H), 7.28 (d, J=8.6Hz, 2H), 5.39 (s, 1H), 3.72 (s, 2H), 3.50 (s, 2H), 3.40
(d, J=13.4Hz, 3H), 3.29-3.22 (m, 4H), 2.93 (s, 2H), 2.50 (d, J=14.8Hz, 2H), 2.22-2.11 (m,
2H),1.42(s,9H).13C NMR(100MHz,D2O)δ173.21(s),152.43(s),146.29(s),140.40(s),
133.22(s),129.55(s,2C),126.81(s,2C),96.33(s),66.53(s),62.48(s,2C),54.27(s,
2C),47.70(s,2C),41.43(s,2C),31.57(s),27.86(s,3C).
III-9:{ 4- [5- bromo- 6- (methylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] first
Keto hydrochloride, white solid, yield: 81.3%, Mp:262~265 DEG C.1H NMR(400MHz,D2O)δ7.98(s,1H),7.32
(d, J=8.6Hz, 2H), 7.19 (d, J=8.6Hz, 2H), 3.59 (d, J=14.9Hz, 8H), 3.32 (d, J=13.3Hz,
2H), 3.25-3.12 (m, 4H), 3.01 (s, 2H), 2.89 (s, 3H), 2.42 (d, J=14.5Hz, 2H), 2.14-2.00 (m,
2H).13C NMR(101MHz,DMSO-d6)δ170.98(s),153.19(s),152.66(s),143.82(s),138.25(s),
130.96(s),127.32(s,2C),124.61(s,2C),91.74(s),60.28(s,2C),59.47(s),45.50(s,
2C),39.24(s,2C),29.38(s),26.21(s,2C).
III-10:{ 4- [5- bromo- 6- (ethylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] first
Keto hydrochloride, white solid, yield: 85.8%, Mp:260~263 DEG C.1H NMR(400MHz,D2O)δ(ppm):7.95(s,
1H), 7.29 (d, J=8.6Hz, 2H), 7.18 (d, J=8.6Hz, 2H), 3.57 (d, J=17.4Hz, 8H), 3.34-3.30 (m,
4H), 3.20-3.14 (m, 4H), 2.96 (br, 2H), 2.41 (d, J=14.5Hz, 2H), 2.10-2.04 (m, 2H), 1.08 (t, J
=7.2Hz, 3H)13C NMR(100MHz,D2O)δ(ppm):173.10(s),155.41(s),154.35(s),146.29(s),
140.49(s),133.11(s),129.49(s),126.79(s),94.03(s),66.50(s),47.68(s),41.43(s),
37.18(s),31.58(s),13.31(s).
III-11:{ 4- [5- bromo- 6- (isopropylamine) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl]
Methanone hvdrochloric acid salt, white solid, yield: 90.2%, Mp:247~249 DEG C.1H NMR(400MHz,D2O)δ(ppm):7.96(s,
1H), 7.31 (d, J=8.3Hz, 2H), 7.19 (d, J=8.4Hz, 2H), 3.95 (dt, J=12.9,6.4Hz, 1H), 3.60-
3.55 (m, 8H), 3.33 (d, J=13.1Hz, 2H), 3.26-3.12 (m, 4H), 2.97 (s, 2H), 2.42 (d, J=14.6Hz,
2H), 2.07 (t, J=12.1Hz, 2H), 1.14 (d, J=6.4Hz, 6H)13C NMR(100MHz,D2O)δ(ppm):173.15
(s),155.45(s),153.90(s),146.42(s),140.44(s),133.14(s),129.49(s,2C),126.78(s,
2C),94.15(s),66.50(s,3C),47.68(s,2C),45.01(s,2C),41.42(s,2C),31.57(s),21.13
(s,2C).
III-12:{ 4- [5- bromo- 6- (tert-butylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidines -4-
Base] methanone hvdrochloric acid salt, white solid, yield: 85.4%, Mp:278~280 DEG C.1H NMR(400MHz,D2O)δ7.94(s,
1H), 7.32 (d, J=8.7Hz, 2H), 7.20 (d, J=8.7Hz, 2H), 3.62 (m, 4H), 3.37-3.33 (m, 3H), 3.27
(br, 2H), 3.19 (t, J=11.8Hz, 3H), 3.05 (br, 2H), 2.45 (d, J=14.4Hz, 2H), 2.15-2.04 (m,
2H),1.29(s,9H).13C NMR(100MHz,D2O)δ173.30(s),148.61(s),140.29(s),133.16(s),
129.46(s,2C),126.81(s,2C),80.63(s),66.52(s),52.06(s,2C),47.72(s,2C),41.45(s,
2C),31.49(s,2C),27.69(s,4C).
Experimental example compound is tested Akt1 inhibitory activity and is surveyed to the growth inhibition of lymphoma mantle cell (MCL) cell strain
Fixed experiment
(1) compound tests Akt1 kinase inhibiting activity:
Experimental material and instrument: TR-FRET enzyme assay kit (German Cisbio company), dimethyl sulfoxide DMSO
(Sigma-Aldrich), electronic analytical balance ER-182A type (Japanese A&D company), Akt1 kinases 200ng/ μ L
(Japanese Carna Biosciences company), 384 microwell plates (Perkin Elmer company of the U.S.), microplate reader (Perkin
Elmer Inspire multi-function microplate reader), carbon dioxide incubator (Forma Scientific company of the U.S.), desk-top centrifugation
Machine (Thermo Scientific company of the U.S.).
Experimental method: under the conditions of 0 DEG C, by the compound of 4 μ L various concentrations, the biotinylated substrate HTRF of 2 μ L
KinEASE STK S2 or S3 (substrate of Akt) and 2 μ L Akt kinases are added sequentially on 384 orifice plates, mix centrifugation, and 2 μ are added
L ATP mixes centrifugation, is incubated for 45 minutes at 37 DEG C.Sequentially add 5 μ L anti-Eu (K)-STK antibody-solutions and 5 μ L
Streptavidin-XL665 buffer (enzyme reaction can be terminated by including EDTA) is incubated at room temperature 1h, makes the phosphoric acid of antibody and substrate
Change site and Streptavidin-XL665 and sufficiently combined with the biotin that substrate is connected, with BioTek multi-function microplate reader
Synnergy 2TMDetect the fluorescent value of launch wavelength 620nm and 665nm.
Setting compound test group (C), positive controls (P) and negative control group (N) are needed in experiment.Test group is will not
Be added in 384 orifice plates with concentration testing compound solution (4 hole μ L/), positive controls then be added same volume 1 × swash
Enzyme buffer liquid, other are identical as test group;Untested compound is not added in negative control group, and Akt1 kinase solution is also not added, with 6 μ L/
1 × the kinase buffer liquid in hole replaces, other are identical as test group.
The calculation formula of inhibiting rate are as follows:
Wherein c is test group, and n is background group, and p is blank group.
With software Graghpad Prism6.0 using the logarithm of concentration as abscissa, inhibiting rate is ordinate matched curve, meter
Calculate IC50。
Target compound the results are shown in Table 1 to Akt1 kinase inhibiting activity measurement experiment.
The inhibitory activity determination data of 1. compound Akt kinases of table
N indicates inactive.
1 experimental data of table shows compound II-2, II-3, II-4, II-8, II-10, II-11, II-12 and III-12 couple
The inhibitory activity of Akt1 is preferable.
(2) compound tests the growth inhibitory activity of lymphoma mantle cell (MCL) cell strain:
Experimental material and instrument:
Cell and cultivate reagent: people lymphoma mantle cell cell strain Mino, Rec-1, Jeko-1, Maver-1, Z-138,
Granta-519, JVM-2, JVM-13 (American type culture collection-American Type Culture
Collection, ATCC), RPMI-1640 culture medium (Sigma Co., USA), fetal calf serum (Sigma Co., USA), HEPES
Buffer (CORNING company of the U.S.), penicillin receive (10000units/mL)-streptomycin sulphate (10mg/mL) (U.S. Sigma
Company), trypan blue reagent-Trypan blue solution (Sigma Co., USA), the inverted light microscope (U.S.
Fisher Scientific company), cell incubator (NUAIER company of the U.S.), superclean bench (NUAIER company of the U.S.),
Cell counter-TC20TMAutomated Cell Counter) (Bio-Rad company of the U.S.), the electric-heated thermostatic water bath (U.S.
Fisher Scientific company), desk centrifuge (Thermo Scientific company of the U.S.), microplate reader (BioTek
Synergy HTX multi-tester), ultra low temperature freezer (Thermo Scientific company of the U.S.).
Experimental method: logarithmic growth phase MCL cell strain is inoculated in 96 well culture plates, and cell number is 1 × 104/ hole,
Be added the surveyed compound of various concentration cell culture fluid, make its final concentration of 0.93-60 μM, at the same set up positive controls with
DMSO blank control group adjusts DMSO concentration≤1 ‰.Each concentration sets 3 multiple holes, finishes, and sets 37 DEG C, 5%CO2Constant temperature incubation
72h is incubated in case.Then 30 μ L CellTiter- are added in every holeReagent, with BioTek Synergy HTX multifunctional examining
It surveys instrument (BioTek, USA) detector and measures its luminance value under 570nm wavelength, institute's value and feminine gender DMSO control group
It is normalized, calculates IC50 value using 6.0 software of Prism (GraphPad Software, USA).Compound inhibits
Rate is by formula: inhibiting rate (IR%)=(blank group OD value-administration group OD value)/blank group OD value × 100%, calculates, further according to
Inhibiting rate concentration curve obtains IC50 value.
Compound is shown in Table 2-1,2-2 to the growth inhibitory activity measurement result of MCL cell strain.
Growth inhibitory activity determination data of the table 2-1. compound to MCL cell strain
aNumerical value is the average value of three groups of independent experiments
Growth inhibitory activity determination data of the table 2-2. compound to MCL cell strain
aNumerical value is the average value of three groups of independent experiments
Table 2-1 experimental data shows that compared with GSK690693, II series compound is obvious to the growth inhibitory activity of MCL
It improves.With activity consistent, compound II-2, II-3, II-4, II-8, II-10 stronger to Akt kinase activity to Akt enzyme
Also relatively strong to the growth inhibitory activity of MCL cell strain, half-inhibitory concentration is all in low micromolar grade (1 μM or so), growth suppression
Activity processed is substantially better than MCL marketed drug according to Shandong for Buddhist nun (Ibrutinib).
Table 2-2 experimental data shows although III series compound loses the inhibitory activity to Akt kinases, wherein big portion
Divide compound all relatively strong to the half growth inhibitory concentration of MCL cell, half growth inhibitory concentration of the majority of compounds to MCL
Lower than 10 μM.Plurality of compound is quite even more excellent to the growth inhibitory activity and GSK690693 of MCL, and activity is preferably changed
Closing object III-8 is low micromolar grade to the half growth inhibitory concentration of MCL cell strain, is much better than GSK690693, and replace Buddhist nun according to Shandong
It is active suitable.
Claims (10)
1. compound shown in a kind of formula (I) or its isomers or solvate or officinal salt:
Wherein, X is selected from H ,-CH- ,-C-Br and halogen;Y is selected from H ,-CH-, C1-C18Linear or branched alkyl group;Between X and YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, containing one or more miscellaneous
Five yuan or hexa-atomic naphthenic base of atom, the hetero atom are selected from O, S and N.
2. compound shown in formula (I) according to claim 1 or its isomers or solvate or officinal salt, feature
It is, X is selected from H ,-CH- ,-C-Br and halogen;Y is selected from H ,-CH- and C1-C8Linear or branched alkyl group;Between X and Y
For no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, containing one or more miscellaneous
Five yuan or hexa-atomic naphthenic base of atom, the hetero atom are selected from O, S and N;
Further, X is selected from H ,-CH- ,-C-Br, F, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X with
Between YFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from amino, substituted-amino, cyano, heteroatomic five yuan containing one or more
Or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;Wherein, the substituted-amino be by tertbutyloxycarbonyl (Boc) and/or
C1-C18Linear or branched alkyl group replaced amino;Wherein, described containing one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base is selected from pyrroles, piperidines, substituted piperidine, morpholine, piperazine and substituted-piperazinyl;
Further, X is selected from H ,-CH- ,-C-Br, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X and Y
BetweenFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from amino, substituted-amino, cyano, heteroatomic five yuan containing one or more
Or hexa-atomic naphthenic base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C8's
Amino replaced linear or branched alkyl group;It is described containing one or more heteroatomic five yuan or hexa-atomic naphthenic base be selected from pyrroles,
Piperidines, substituted piperidine, morpholine, piperazine and substituted-piperazinyl;
Further, the substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Linear chain or branched chain alkyl, ammonia
Base, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, X is selected from H ,-CH- ,-C-Br, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X and Y
BetweenFor no key or double bond;
R1Selected from-CHR2AndWherein, R2Selected from amino, substituted-amino, containing one or more heteroatomic five yuan or hexa-atomic
Naphthenic base, the hetero atom are selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C3Straight chain or
Amino replaced branched alkyl;It is described to be selected from pyrroles containing one or more heteroatomic five yuan or hexa-atomic naphthenic base, piperidines, take
For piperidines, morpholine, piperazine and substituted-piperazinyl;The substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Straight chain or
The alkyl of branch, amino, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, the substituted-amino is selected from
Further, the substituted piperidine is selected from
Further, the substituted-piperazinyl is selected from
Further, X is selected from H ,-CH- ,-C-Br, Cl and Br;Y is selected from H ,-CH- and C1-C5Linear or branched alkyl group;X and Y
BetweenFor no key or double bond;
R1Selected from-CHR2AndWherein, R2It is selected from
3. compound according to claim 1 or 2 or its isomers or solvate or officinal salt, which is characterized in that X
Between YFor double bond, X is selected from-CH- and-C-Br;Y is-CH-;
Further, the compound has structure as follows:
Wherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base, the hetero atom are selected from O, S and N;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic naphthenic base, institute
It states hetero atom and is selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C18Linear or branched alkyl group
Replaced amino;It is described containing one or more heteroatomic five yuan or hexa-atomic naphthenic base be selected from pyrroles, piperidines, substituted piperidine,
Morpholine, piperazine and substituted-piperazinyl;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic naphthenic base, institute
It states hetero atom and is selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C8Linear or branched alkyl group institute
Substituted amino;It is described containing one or more heteroatomic five yuan or hexa-atomic naphthenic base be selected from pyrroles, piperidines, substituted piperidine,
Quinoline, piperazine and substituted-piperazinyl;
Further, the substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Linear chain or branched chain alkyl, ammonia
Base, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, the substituted-amino is selected from
Further, the substituted piperidine is selected from
Further, the substituted-piperazinyl is selected from
Further, R2It is selected from
Further, between X and YFor no key;X is selected from H and halogen;Y is C1-C18Linear or branched alkyl group;
Further, R1For
Further, the compound has structure as follows:
Wherein, X is selected from H, F, Cl, Br;Y is C1-C8Linear or branched alkyl group;
Further, X is selected from H, F, Cl, Br;Y is C1-C5Linear or branched alkyl group;
Further, X H, Cl or Br;Y is methyl, ethyl, isopropyl or tert-butyl.
4. formula (I) compound according to any one of claim 1 to 3 or its isomers or solvate or pharmaceutically acceptable
Salt, which is characterized in that it is selected from flowering structure:
Tert-butyl { 2- [4- (the bromo- 7H- pyrroles of 5- [2,3-d] pyrimidine-4-yl) piperazine -1- base] -1- (4- chlorphenyl) -2- oxygen second
Base } carbamate (II-1);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (dimethylamino) second
Ketone (II-2);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (lignocaine) second
Ketone (II-3);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (pyrroles -1- base) second
Ketone (II-4);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (3,5- dimethyl piperazine
Pyridine -1- base) ethyl ketone (II-5);
1- [4- (5- bromo- 7H- [2,3-d] pyrimidine-4-yl) piperazinyl] -2- (4- chlorphenyl) -2- morpholine ethyl ketone (II-6);
Tert-butyl 4- { 2- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -1- (4- chlorphenyl } -2- oxygen second
Base) piperazine -1- carboxylate (II-7);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (4- methyl piperazine
Base) ethyl ketone (II-8);
Tert-butyl { { 1- { 2- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -1- (4- chlorphenyl) -2- oxygen
Ethyl } piperidin-4-yl } methyl } carbamate (II-9);
2- amino -1- (4- (the bromo- 7H- pyrroles of 5- [2,3-d] pyrimidine-4-yl) piperazine -1- base) -2- (4- chlorobenzene) acetophenone hydrochloride
(II-10);
1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2- (4- chlorphenyl) -2- (piperazinyl) ethyl ketone
Hydrochloride (II-11);
2- [4- (amino methyl) piperidin-1-yl) -1- [4- (bromo- 7H- pyrrolo- [2,3-d] pyrimidine-4-yl of 5-) piperazinyl] -2-
(4- chlorphenyl) acetophenone hydrochloride (II-12);
[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (methylamino) pyrimidine-4-yl] piperazinyl } methanone hvdrochloric acid salt (III-
1);
[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (ethylamino) pyrimidine-4-yl] piperazinyl } methanone hvdrochloric acid salt (III-2);
[4- (4- chlorphenyl) piperidin-4-yl] { 4- [6- (isopropylamine) pyrimidine-4-yl] piperazinyl } methanone hvdrochloric acid salt (III-
3);
4- [6- (tert-butylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt (III-
4);
{ 4- [5- chloro- 6- (methylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-5);
{ 4- [5- chloro- 6- (ethylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-6);
{ 4- [5- chloro- 6- (isopropylamine) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-7);
{ 4- [6- (tert-butylamino) -5- chlorine pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-8);
{ 4- [5- bromo- 6- (methylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-9);
{ 4- [5- bromo- 6- (ethylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-10);
{ 4- [5- bromo- 6- (isopropylamine) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-11);
{ 4- [5- bromo- 6- (tert-butylamino) pyrimidine-4-yl] piperazinyl } [4- (4- chlorphenyl) piperidin-4-yl] methanone hvdrochloric acid salt
(III-12)。
5. a kind of method for preparing compound or pharmaceutically acceptable salt thereof shown in formula (II), the method reaction route as described below
(reaction route 1) carries out:
Wherein, R2Selected from halogen, nitro, amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic cycloalkanes
Base, the hetero atom are selected from O, S and N;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic naphthenic base, institute
It states hetero atom and is selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C18Linear or branched alkyl group
Replaced amino;It is described containing one or more heteroatomic five yuan or hexa-atomic naphthenic base be selected from pyrroles, piperidines, substituted piperidine,
Morpholine, piperazine and substituted-piperazinyl;
Further, R2Selected from amino, substituted-amino, cyano, contain one or more heteroatomic five yuan or hexa-atomic naphthenic base, institute
It states hetero atom and is selected from O, S and N;The substituted-amino is by tertbutyloxycarbonyl (Boc) and/or C1-C8Linear or branched alkyl group institute
Substituted amino;It is described containing one or more heteroatomic five yuan or hexa-atomic naphthenic base be selected from pyrroles, piperidines, substituted piperidine,
Quinoline, piperazine and substituted-piperazinyl;
Further, the substituted piperidine or substituted-piperazinyl are each independently selected from by C1-C5Linear chain or branched chain alkyl, ammonia
Base, the amino and tertbutyloxycarbonyl replaced by tertbutyloxycarbonyl;
Further, the substituted-amino is selected from
Further, the substituted piperidine is selected from
Further, the substituted-piperazinyl is selected from
Further, R2It is selected from
Further, which comprises with starting material 1 in DMF (n,N-Dimethylformamide) with NBS (N- bromo amber
Amber acid imide) react to obtain intermediate 2;Intermediate 2,1-Boc- piperazine and DIEA (N, N- diisopropylethylamine) react in DMF
Generate intermediate 3;Intermediate 3 reacts in methanol solution with hydrogen chloride dioxane solution, takes off Boc protecting group, obtains intermediate
Body 4;Intermediate 4 is in EDCI (1- (3- dimethylamino-propyl) -3- ethyl-carbodiimide hydrochloride), HOBt (1- hydroxy benzo three
Azoles), under DIEA and DMF existence condition, after reacting with intermediate acid M, obtain formula (II) compound;And/or further, with
The methanol solution of formula (II) compound arrived is reacted with the dioxane solution of hydrogen chloride, obtains formula (II) compound newly;
Further, the intermediate acid M has structure as follows:
Wherein, R2It is selected from
6. a kind of method for preparing compound or pharmaceutically acceptable salt thereof shown in formula (III), the method reaction route as described below
(reaction route 2) carries out:
Wherein, X is selected from H, F, Cl, Br;Y is C1-C8Linear or branched alkyl group;
Further, X is selected from H, F, Cl, Br;Y is C1-C5Linear or branched alkyl group;
Further, X H, Cl or Br;Y is methyl, ethyl, isopropyl or tert-butyl;
Further, which comprises be dissolved in isopropanol with starting material 5, react to obtain intermediate 6a-6d with amine is replaced;
Intermediate 6a-6d and 1-Boc- piperazine are in dioxane and K2CO3In the presence of reaction generate intermediate 7a-7d;Intermediate 7a-7d
It under glacial acetic acid existence condition, is reacted with NCS/NBS, obtains intermediate 7e-7l;Intermediate 7e-7l is in methanol solution, with chlorination
The reaction of hydrogen dioxane solution, takes off Boc protecting group, obtains intermediate 8a-8l;Intermediate 8a-8l in EDCI, HOBt, DIEA and
After reacting in the presence of DMF with intermediate acid N, intermediate 9a-9l is obtained;By the methanol solution of intermediate 9a-9l, with hydrogen chloride two
Six ring solution reaction of oxygen, obtains the hydrochloride of formula (III) compound;
Further, the intermediate acid N is
7. a kind of pharmaceutical composition, it includes formula (I) compounds or its isomers or solvation described in claims 1 or 2
Object or officinal salt or formula as claimed in claim 3 (II) or formula (III) compound or its isomers or solvate can medicines
Any one compound described in salt or claim 4 or its isomers or solvate or officinal salt.
8. (I) compound of formula described in claims 1 or 2 or its isomers or solvate or officinal salt or right are wanted
Institute in formula described in asking 3 (II) or formula (III) compound or its isomers or solvate or officinal salt or claim 4
Any one compound or its isomers or solvate or officinal salt stated or pharmaceutical composition as claimed in claim 7 exist
Prepare the application in Akt inhibitor.
9. (I) compound of formula described in claims 1 or 2 or its isomers or solvate or officinal salt or right are wanted
Institute in formula described in asking 3 (II) or formula (III) compound or its isomers or solvate or officinal salt or claim 4
Any one compound or its isomers or solvate or officinal salt stated or pharmaceutical composition as claimed in claim 7 exist
Prepare the application in anti-tumor drug;
Further, the tumour is lymphoma mantle cell.
10. a kind of drug combination combination comprising (I) compound of formula described in claims 1 or 2 or its isomers or solvent
Compound or officinal salt or formula as claimed in claim 3 (II) or formula (III) compound or its isomers or solvate can
Any one compound described in pharmaceutical salts or claim 4 or its isomers or solvate or officinal salt or right are wanted
The use in conjunction of pharmaceutical composition described in asking 7 and anti-tumor drug.
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